ENST00000281928.9:c.5036T>G
MANE Select
|
ENSP00000281928.3:p.Ile1679Ser
|
|
ENST00000549786.2:c.4464T>G
|
|
|
ENST00000648379.1:n.3404T>G
|
|
|
ENST00000648737.1:n.4800T>G
|
|
|
ENST00000648825.1:n.1776T>G
|
|
|
ENST00000648916.1:n.3047T>G
|
|
|
ENST00000649146.1:n.2279T>G
|
|
|
ENST00000649607.1:c.3220T>G
|
|
|
ENST00000649775.1:c.1525T>G
|
|
|
ENST00000650226.1:c.5036T>G
|
ENSP00000496981.1:p.Ile1679Ser
|
|
ENST00000281928.7:c.5036T>G
|
ENSP00000281928.3:p.Ile1679Ser
|
|
ENST00000549786.1:c.400T>G
|
|
|
ENST00000552340.1:c.68T>G
|
ENSP00000449876.1:p.Ile23Ser
|
|
NM_015335.4:c.5036T>G
|
NP_056150.1:p.Ile1679Ser
|
|
XM_011538080.1:c.5036T>G
|
XP_011536382.1:p.Ile1679Ser
|
|
XM_011538081.1:c.5033T>G
|
XP_011536383.1:p.Ile1678Ser
|
|
XM_011538082.1:c.5006T>G
|
XP_011536384.1:p.Ile1669Ser
|
|
XM_011538080.2:c.5036T>G
|
XP_011536382.1:p.Ile1679Ser
|
|
XM_011538081.2:c.5033T>G
|
XP_011536383.1:p.Ile1678Ser
|
|
XM_011538082.2:c.5006T>G
|
XP_011536384.1:p.Ile1669Ser
|
|
XM_017019090.1:c.5033T>G
|
XP_016874579.1:p.Ile1678Ser
|
|
NM_015335.5:c.5036T>G
MANE Select
|
NP_056150.1:p.Ile1679Ser
|
|