ENST00000265104.5:c.9774G>T
MANE Select
|
ENSP00000265104.4:p.Glu3258Asp
|
|
ENST00000681290.1:c.9729G>T
|
ENSP00000505288.1:p.Glu3243Asp
|
|
ENST00000265104.4:c.9774G>T
|
ENSP00000265104.4:p.Glu3258Asp
|
|
ENST00000504001.3:n.486G>T
|
|
|
NM_001369.2:c.9774G>T
|
NP_001360.1:p.Glu3258Asp
|
|
XM_005248262.2:c.9729G>T
|
XP_005248319.1:p.Glu3243Asp
|
|
XM_005248262.3:c.9882G>T
|
XP_005248319.2:p.Glu3294Asp
|
|
XM_017009177.1:c.9882G>T
|
XP_016864666.1:p.Glu3294Asp
|
|
XM_017009178.1:c.8787G>T
|
XP_016864667.1:p.Glu2929Asp
|
|
XM_017009179.2:c.8787G>T
|
XP_016864668.1:p.Glu2929Asp
|
|
XM_017009180.1:c.9882G>T
|
XP_016864669.1:p.Glu3294Asp
|
|
XM_017009181.1:c.9882G>T
|
XP_016864670.1:p.Glu3294Asp
|
|
XM_017009182.1:c.9882G>T
|
XP_016864671.1:p.Glu3294Asp
|
|
XM_017009185.1:c.4971G>T
|
XP_016864674.1:p.Glu1657Asp
|
|
XM_017009186.1:c.4524G>T
|
XP_016864675.1:p.Glu1508Asp
|
|
XM_017009188.1:c.3861G>T
|
XP_016864677.1:p.Glu1287Asp
|
|
XM_024454388.1:c.8787G>T
|
XP_024310156.1:p.Glu2929Asp
|
|
XM_024454389.1:c.8376G>T
|
XP_024310157.1:p.Glu2792Asp
|
|
NM_001369.3:c.9774G>T
MANE Select
|
NP_001360.1:p.Glu3258Asp
|
|