ENST00000281928.9:c.4355A>C
MANE Select
|
ENSP00000281928.3:p.Gln1452Pro
|
|
ENST00000549786.2:c.3783A>C
|
|
|
ENST00000648379.1:n.2723A>C
|
|
|
ENST00000648737.1:n.4119A>C
|
|
|
ENST00000648825.1:n.1095A>C
|
|
|
ENST00000648916.1:n.2366A>C
|
|
|
ENST00000649146.1:n.1085A>C
|
|
|
ENST00000649607.1:c.2539A>C
|
|
|
ENST00000649775.1:c.852A>C
|
|
|
ENST00000650091.1:n.2331A>C
|
|
|
ENST00000650226.1:c.4355A>C
|
ENSP00000496981.1:p.Gln1452Pro
|
|
ENST00000281928.7:c.4355A>C
|
ENSP00000281928.3:p.Gln1452Pro
|
|
NM_015335.4:c.4355A>C
|
NP_056150.1:p.Gln1452Pro
|
|
XM_011538080.1:c.4355A>C
|
XP_011536382.1:p.Gln1452Pro
|
|
XM_011538081.1:c.4352A>C
|
XP_011536383.1:p.Gln1451Pro
|
|
XM_011538082.1:c.4325A>C
|
XP_011536384.1:p.Gln1442Pro
|
|
XM_011538080.2:c.4355A>C
|
XP_011536382.1:p.Gln1452Pro
|
|
XM_011538081.2:c.4352A>C
|
XP_011536383.1:p.Gln1451Pro
|
|
XM_011538082.2:c.4325A>C
|
XP_011536384.1:p.Gln1442Pro
|
|
XM_017019090.1:c.4352A>C
|
XP_016874579.1:p.Gln1451Pro
|
|
NM_015335.5:c.4355A>C
MANE Select
|
NP_056150.1:p.Gln1452Pro
|
|