ENST00000281928.9:c.5021C>A
MANE Select
|
ENSP00000281928.3:p.Pro1674His
|
|
ENST00000549786.2:c.4449C>A
|
|
|
ENST00000648379.1:n.3389C>A
|
|
|
ENST00000648737.1:n.4785C>A
|
|
|
ENST00000648825.1:n.1761C>A
|
|
|
ENST00000648916.1:n.3032C>A
|
|
|
ENST00000649146.1:n.2264C>A
|
|
|
ENST00000649607.1:c.3205C>A
|
|
|
ENST00000649775.1:c.1510C>A
|
|
|
ENST00000650226.1:c.5021C>A
|
ENSP00000496981.1:p.Pro1674His
|
|
ENST00000281928.7:c.5021C>A
|
ENSP00000281928.3:p.Pro1674His
|
|
ENST00000549786.1:c.385C>A
|
|
|
ENST00000552340.1:c.53C>A
|
ENSP00000449876.1:p.Pro18His
|
|
NM_015335.4:c.5021C>A
|
NP_056150.1:p.Pro1674His
|
|
XM_011538080.1:c.5021C>A
|
XP_011536382.1:p.Pro1674His
|
|
XM_011538081.1:c.5018C>A
|
XP_011536383.1:p.Pro1673His
|
|
XM_011538082.1:c.4991C>A
|
XP_011536384.1:p.Pro1664His
|
|
XM_011538080.2:c.5021C>A
|
XP_011536382.1:p.Pro1674His
|
|
XM_011538081.2:c.5018C>A
|
XP_011536383.1:p.Pro1673His
|
|
XM_011538082.2:c.4991C>A
|
XP_011536384.1:p.Pro1664His
|
|
XM_017019090.1:c.5018C>A
|
XP_016874579.1:p.Pro1673His
|
|
NM_015335.5:c.5021C>A
MANE Select
|
NP_056150.1:p.Pro1674His
|
|