ENST00000375708.4:c.2787T>A
MANE Select
|
ENSP00000364860.3:p.Cys929Ter
|
|
ENST00000375708.3:c.2787T>A
|
ENSP00000364860.3:p.Cys929Ter
|
|
ENST00000375715.5:c.1920+447T>A
|
ENSP00000364867.1:n.1920+447T>A
|
|
ENST00000550066.5:n.3255T>A
|
|
|
NM_004560.3:c.2787T>A
|
NP_004551.2:p.Cys929Ter
|
|
XM_005252008.3:c.2367T>A
|
XP_005252065.1:p.Cys789Ter
|
|
XM_005252009.3:c.1584T>A
|
XP_005252066.1:p.Cys528Ter
|
|
XM_006717121.2:c.2367T>A
|
XP_006717184.1:p.Cys789Ter
|
|
XM_011518721.1:c.2367T>A
|
XP_011517023.1:p.Cys789Ter
|
|
XM_005252008.4:c.2367T>A
|
XP_005252065.1:p.Cys789Ter
|
|
XM_006717121.3:c.2367T>A
|
XP_006717184.1:p.Cys789Ter
|
|
XM_017014762.1:c.2778T>A
|
XP_016870251.1:p.Cys926Ter
|
|
XM_017014763.1:c.2367T>A
|
XP_016870252.1:p.Cys789Ter
|
|
NM_004560.4:c.2787T>A
MANE Select
|
NP_004551.2:p.Cys929Ter
|
|