ENST00000234071.8:c.555G>A
MANE Select
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ENSP00000234071.4:p.Arg185=
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ENST00000234071.7:c.555G>A
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ENSP00000234071.3:p.Arg185=
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ENST00000402125.2:c.121-2253G>A
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|
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ENST00000409048.1:c.657G>A
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ENSP00000386679.1:p.Arg219=
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ENST00000442644.5:c.498G>A
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ENSP00000411241.1:p.Arg166=
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ENST00000464089.1:n.141G>A
|
|
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NM_000312.3:c.555G>A , LRG_599t1:c.555G>A
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NP_000303.1:p.Arg185=
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|
XM_005263715.3:c.738G>A
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XP_005263772.1:p.Arg246=
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XM_005263716.3:c.720G>A
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XP_005263773.1:p.Arg240=
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XM_005263717.3:c.618G>A
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XP_005263774.1:p.Arg206=
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XM_005263717.4:c.618G>A
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XP_005263774.1:p.Arg206=
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XM_017004505.1:c.798G>A
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XP_016859994.1:p.Arg266=
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XM_024453002.1:c.900G>A
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XP_024308770.1:p.Arg300=
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XM_024453003.1:c.840G>A
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XP_024308771.1:p.Arg280=
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XM_024453004.1:c.738G>A
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XP_024308772.1:p.Arg246=
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XM_024453005.1:c.720G>A
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XP_024308773.1:p.Arg240=
|
|
XM_024453006.1:c.657G>A
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XP_024308774.1:p.Arg219=
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XR_923313.2:n.4481C>T
|
|
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NM_000312.4:c.555G>A
MANE Select
|
NP_000303.1:p.Arg185=
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|
NM_001375602.1:c.738G>A
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NP_001362531.1:p.Arg246=
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NM_001375603.1:c.720G>A
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NP_001362532.1:p.Arg240=
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|
NM_001375604.1:c.618G>A
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NP_001362533.1:p.Arg206=
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NM_001375605.1:c.657G>A
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NP_001362534.1:p.Arg219=
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NM_001375606.1:c.723G>A
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NP_001362535.1:p.Arg241=
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NM_001375607.1:c.741G>A
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NP_001362536.1:p.Arg247=
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NM_001375608.1:c.498G>A
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NP_001362537.1:p.Arg166=
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NM_001375609.1:c.531G>A
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NP_001362538.1:p.Arg177=
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NM_001375610.1:c.549G>A
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NP_001362539.1:p.Arg183=
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NM_001375611.1:c.555G>A
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NP_001362540.1:p.Arg185=
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NM_001375613.1:c.555G>A
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NP_001362542.1:p.Arg185=
|
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