ENST00000234071.8:c.881G>T
MANE Select
|
ENSP00000234071.4:p.Ser294Ile
|
|
ENST00000234071.7:c.881G>T
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ENSP00000234071.3:p.Ser294Ile
|
|
ENST00000402125.2:c.205G>T
|
|
|
ENST00000409048.1:c.983G>T
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ENSP00000386679.1:p.Ser328Ile
|
|
NM_000312.3:c.881G>T , LRG_599t1:c.881G>T
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NP_000303.1:p.Ser294Ile
|
|
XM_005263715.3:c.1064G>T
|
XP_005263772.1:p.Ser355Ile
|
|
XM_005263716.3:c.1046G>T
|
XP_005263773.1:p.Ser349Ile
|
|
XM_005263717.3:c.944G>T
|
XP_005263774.1:p.Ser315Ile
|
|
XR_923313.1:n.1332-177C>A
|
|
|
XM_005263717.4:c.944G>T
|
XP_005263774.1:p.Ser315Ile
|
|
XM_017004505.1:c.1124G>T
|
XP_016859994.1:p.Ser375Ile
|
|
XM_024453002.1:c.1226G>T
|
XP_024308770.1:p.Ser409Ile
|
|
XM_024453003.1:c.1166G>T
|
XP_024308771.1:p.Ser389Ile
|
|
XM_024453004.1:c.1064G>T
|
XP_024308772.1:p.Ser355Ile
|
|
XM_024453005.1:c.1046G>T
|
XP_024308773.1:p.Ser349Ile
|
|
XM_024453006.1:c.983G>T
|
XP_024308774.1:p.Ser328Ile
|
|
XR_001739705.1:n.3607-177C>A
|
|
|
XR_923313.2:n.4043-177C>A
|
|
|
NM_000312.4:c.881G>T
MANE Select
|
NP_000303.1:p.Ser294Ile
|
|
NM_001375602.1:c.1064G>T
|
NP_001362531.1:p.Ser355Ile
|
|
NM_001375603.1:c.1046G>T
|
NP_001362532.1:p.Ser349Ile
|
|
NM_001375604.1:c.944G>T
|
NP_001362533.1:p.Ser315Ile
|
|
NM_001375605.1:c.983G>T
|
NP_001362534.1:p.Ser328Ile
|
|
NM_001375606.1:c.1049G>T
|
NP_001362535.1:p.Ser350Ile
|
|
NM_001375607.1:c.1067G>T
|
NP_001362536.1:p.Ser356Ile
|
|
NM_001375608.1:c.824G>T
|
NP_001362537.1:p.Ser275Ile
|
|
NM_001375609.1:c.857G>T
|
NP_001362538.1:p.Ser286Ile
|
|
NM_001375610.1:c.875G>T
|
NP_001362539.1:p.Ser292Ile
|
|
NM_001375611.1:c.881G>T
|
NP_001362540.1:p.Ser294Ile
|
|
NM_001375613.1:c.881G>T
|
NP_001362542.1:p.Ser294Ile
|
|