ENST00000370096.9:c.2649T>C
MANE Select
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ENSP00000359114.3:p.Gly883=
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ENST00000353414.8:c.2532T>C
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ENSP00000302551.6:p.Gly844=
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ENST00000358392.6:c.2685T>C
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ENSP00000351163.2:p.Gly895=
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ENST00000370096.7:c.2649T>C
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ENSP00000359114.3:p.Gly883=
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ENST00000512756.5:c.2301T>C
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ENSP00000426533.1:p.Gly767=
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ENST00000635193.1:c.1983T>C
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|
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NM_001190709.1:c.2532T>C
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NP_001177638.1:p.Gly844=
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NM_001854.3:c.2649T>C
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NP_001845.3:p.Gly883=
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NM_080629.2:c.2685T>C
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NP_542196.2:p.Gly895=
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NM_080630.3:c.2301T>C
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NP_542197.3:p.Gly767=
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XM_011540719.1:c.2649T>C
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XP_011539021.1:p.Gly883=
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XM_011540720.1:c.882T>C
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XP_011539022.1:p.Gly294=
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XM_011540721.1:c.237T>C
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XP_011539023.1:p.Gly79=
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XR_946545.1:n.3063T>C
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|
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NR_134980.1:n.2983T>C
|
|
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XM_017000334.1:c.2802T>C
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XP_016855823.1:p.Gly934=
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XM_017000335.1:c.2796T>C
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XP_016855824.1:p.Gly932=
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XM_017000336.1:c.2802T>C
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XP_016855825.1:p.Gly934=
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XM_017000337.1:c.1200T>C
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XP_016855826.1:p.Gly400=
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NM_001854.4:c.2649T>C
MANE Select
|
NP_001845.3:p.Gly883=
|
|
NM_080630.4:c.2301T>C
|
NP_542197.3:p.Gly767=
|
|
NR_134980.2:n.3009T>C
|
|
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NM_001190709.2:c.2532T>C
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NP_001177638.1:p.Gly844=
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|
NM_080629.3:c.2685T>C
|
NP_542196.2:p.Gly895=
|
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