ENST00000375708.4:c.2683G>T
MANE Select
|
ENSP00000364860.3:p.Asp895Tyr
|
|
ENST00000375708.3:c.2683G>T
|
ENSP00000364860.3:p.Asp895Tyr
|
|
ENST00000375715.5:c.1920+343G>T
|
ENSP00000364867.1:n.1920+343G>T
|
|
ENST00000550066.5:n.3151G>T
|
|
|
NM_004560.3:c.2683G>T
|
NP_004551.2:p.Asp895Tyr
|
|
XM_005252008.3:c.2263G>T
|
XP_005252065.1:p.Asp755Tyr
|
|
XM_005252009.3:c.1480G>T
|
XP_005252066.1:p.Asp494Tyr
|
|
XM_006717121.2:c.2263G>T
|
XP_006717184.1:p.Asp755Tyr
|
|
XM_011518721.1:c.2263G>T
|
XP_011517023.1:p.Asp755Tyr
|
|
XM_005252008.4:c.2263G>T
|
XP_005252065.1:p.Asp755Tyr
|
|
XM_006717121.3:c.2263G>T
|
XP_006717184.1:p.Asp755Tyr
|
|
XM_017014762.1:c.2674G>T
|
XP_016870251.1:p.Asp892Tyr
|
|
XM_017014763.1:c.2263G>T
|
XP_016870252.1:p.Asp755Tyr
|
|
NM_004560.4:c.2683G>T
MANE Select
|
NP_004551.2:p.Asp895Tyr
|
|