ENST00000375708.4:c.2629G>T
MANE Select
|
ENSP00000364860.3:p.Ala877Ser
|
|
ENST00000375708.3:c.2629G>T
|
ENSP00000364860.3:p.Ala877Ser
|
|
ENST00000375715.5:c.1920+289G>T
|
ENSP00000364867.1:n.1920+289G>T
|
|
ENST00000550066.5:n.3097G>T
|
|
|
NM_004560.3:c.2629G>T
|
NP_004551.2:p.Ala877Ser
|
|
XM_005252008.3:c.2209G>T
|
XP_005252065.1:p.Ala737Ser
|
|
XM_005252009.3:c.1426G>T
|
XP_005252066.1:p.Ala476Ser
|
|
XM_006717121.2:c.2209G>T
|
XP_006717184.1:p.Ala737Ser
|
|
XM_011518721.1:c.2209G>T
|
XP_011517023.1:p.Ala737Ser
|
|
XM_005252008.4:c.2209G>T
|
XP_005252065.1:p.Ala737Ser
|
|
XM_006717121.3:c.2209G>T
|
XP_006717184.1:p.Ala737Ser
|
|
XM_017014762.1:c.2620G>T
|
XP_016870251.1:p.Ala874Ser
|
|
XM_017014763.1:c.2209G>T
|
XP_016870252.1:p.Ala737Ser
|
|
NM_004560.4:c.2629G>T
MANE Select
|
NP_004551.2:p.Ala877Ser
|
|