ENST00000375708.4:c.2767A>G
MANE Select
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ENSP00000364860.3:p.Thr923Ala
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ENST00000375708.3:c.2767A>G
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ENSP00000364860.3:p.Thr923Ala
|
|
ENST00000375715.5:c.1920+427A>G
|
ENSP00000364867.1:n.1920+427A>G
|
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ENST00000550066.5:n.3235A>G
|
|
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NM_004560.3:c.2767A>G
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NP_004551.2:p.Thr923Ala
|
|
XM_005252008.3:c.2347A>G
|
XP_005252065.1:p.Thr783Ala
|
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XM_005252009.3:c.1564A>G
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XP_005252066.1:p.Thr522Ala
|
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XM_006717121.2:c.2347A>G
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XP_006717184.1:p.Thr783Ala
|
|
XM_011518721.1:c.2347A>G
|
XP_011517023.1:p.Thr783Ala
|
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XM_005252008.4:c.2347A>G
|
XP_005252065.1:p.Thr783Ala
|
|
XM_006717121.3:c.2347A>G
|
XP_006717184.1:p.Thr783Ala
|
|
XM_017014762.1:c.2758A>G
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XP_016870251.1:p.Thr920Ala
|
|
XM_017014763.1:c.2347A>G
|
XP_016870252.1:p.Thr783Ala
|
|
NM_004560.4:c.2767A>G
MANE Select
|
NP_004551.2:p.Thr923Ala
|
|