ENST00000281928.9:c.4993C>A
MANE Select
|
ENSP00000281928.3:p.Pro1665Thr
|
|
ENST00000549786.2:c.4421C>A
|
|
|
ENST00000648379.1:n.3361C>A
|
|
|
ENST00000648737.1:n.4757C>A
|
|
|
ENST00000648825.1:n.1733C>A
|
|
|
ENST00000648916.1:n.3004C>A
|
|
|
ENST00000649146.1:n.2236C>A
|
|
|
ENST00000649607.1:c.3177C>A
|
|
|
ENST00000649775.1:c.1482C>A
|
|
|
ENST00000650226.1:c.4993C>A
|
ENSP00000496981.1:p.Pro1665Thr
|
|
ENST00000281928.7:c.4993C>A
|
ENSP00000281928.3:p.Pro1665Thr
|
|
ENST00000549786.1:c.357C>A
|
|
|
ENST00000552340.1:c.25C>A
|
ENSP00000449876.1:p.Pro9Thr
|
|
NM_015335.4:c.4993C>A
|
NP_056150.1:p.Pro1665Thr
|
|
XM_011538080.1:c.4993C>A
|
XP_011536382.1:p.Pro1665Thr
|
|
XM_011538081.1:c.4990C>A
|
XP_011536383.1:p.Pro1664Thr
|
|
XM_011538082.1:c.4963C>A
|
XP_011536384.1:p.Pro1655Thr
|
|
XM_011538080.2:c.4993C>A
|
XP_011536382.1:p.Pro1665Thr
|
|
XM_011538081.2:c.4990C>A
|
XP_011536383.1:p.Pro1664Thr
|
|
XM_011538082.2:c.4963C>A
|
XP_011536384.1:p.Pro1655Thr
|
|
XM_017019090.1:c.4990C>A
|
XP_016874579.1:p.Pro1664Thr
|
|
NM_015335.5:c.4993C>A
MANE Select
|
NP_056150.1:p.Pro1665Thr
|
|