ENST00000281928.9:c.5001T>A
MANE Select
|
ENSP00000281928.3:p.Ser1667=
|
|
ENST00000549786.2:c.4429T>A
|
|
|
ENST00000648379.1:n.3369T>A
|
|
|
ENST00000648737.1:n.4765T>A
|
|
|
ENST00000648825.1:n.1741T>A
|
|
|
ENST00000648916.1:n.3012T>A
|
|
|
ENST00000649146.1:n.2244T>A
|
|
|
ENST00000649607.1:c.3185T>A
|
|
|
ENST00000649775.1:c.1490T>A
|
|
|
ENST00000650226.1:c.5001T>A
|
ENSP00000496981.1:p.Ser1667=
|
|
ENST00000281928.7:c.5001T>A
|
ENSP00000281928.3:p.Ser1667=
|
|
ENST00000549786.1:c.365T>A
|
|
|
ENST00000552340.1:c.33T>A
|
ENSP00000449876.1:p.Ser11=
|
|
NM_015335.4:c.5001T>A
|
NP_056150.1:p.Ser1667=
|
|
XM_011538080.1:c.5001T>A
|
XP_011536382.1:p.Ser1667=
|
|
XM_011538081.1:c.4998T>A
|
XP_011536383.1:p.Ser1666=
|
|
XM_011538082.1:c.4971T>A
|
XP_011536384.1:p.Ser1657=
|
|
XM_011538080.2:c.5001T>A
|
XP_011536382.1:p.Ser1667=
|
|
XM_011538081.2:c.4998T>A
|
XP_011536383.1:p.Ser1666=
|
|
XM_011538082.2:c.4971T>A
|
XP_011536384.1:p.Ser1657=
|
|
XM_017019090.1:c.4998T>A
|
XP_016874579.1:p.Ser1666=
|
|
NM_015335.5:c.5001T>A
MANE Select
|
NP_056150.1:p.Ser1667=
|
|