ENST00000281928.9:c.5101T>A
MANE Select
|
ENSP00000281928.3:p.Leu1701Met
|
|
ENST00000549786.2:c.4529T>A
|
|
|
ENST00000648379.1:n.3469T>A
|
|
|
ENST00000648737.1:n.4865T>A
|
|
|
ENST00000648825.1:n.1841T>A
|
|
|
ENST00000648916.1:n.3112T>A
|
|
|
ENST00000649146.1:n.2344T>A
|
|
|
ENST00000649607.1:c.3285T>A
|
|
|
ENST00000649775.1:c.1590T>A
|
|
|
ENST00000650226.1:c.5101T>A
|
ENSP00000496981.1:p.Leu1701Met
|
|
ENST00000281928.7:c.5101T>A
|
ENSP00000281928.3:p.Leu1701Met
|
|
ENST00000549786.1:c.465T>A
|
|
|
ENST00000552340.1:c.133T>A
|
ENSP00000449876.1:p.Leu45Met
|
|
NM_015335.4:c.5101T>A
|
NP_056150.1:p.Leu1701Met
|
|
XM_011538080.1:c.5101T>A
|
XP_011536382.1:p.Leu1701Met
|
|
XM_011538081.1:c.5098T>A
|
XP_011536383.1:p.Leu1700Met
|
|
XM_011538082.1:c.5071T>A
|
XP_011536384.1:p.Leu1691Met
|
|
XM_011538080.2:c.5101T>A
|
XP_011536382.1:p.Leu1701Met
|
|
XM_011538081.2:c.5098T>A
|
XP_011536383.1:p.Leu1700Met
|
|
XM_011538082.2:c.5071T>A
|
XP_011536384.1:p.Leu1691Met
|
|
XM_017019090.1:c.5098T>A
|
XP_016874579.1:p.Leu1700Met
|
|
NM_015335.5:c.5101T>A
MANE Select
|
NP_056150.1:p.Leu1701Met
|
|