ENST00000281928.9:c.5175+136G>T
MANE Select
|
ENSP00000281928.3:n.5175+136G>T
|
|
ENST00000549786.2:c.4739G>T
|
|
|
ENST00000648379.1:n.3543+136G>T
|
|
|
ENST00000648737.1:n.4939+136G>T
|
|
|
ENST00000648825.1:n.2051G>T
|
|
|
ENST00000648916.1:n.3186+136G>T
|
|
|
ENST00000649146.1:n.2554G>T
|
|
|
ENST00000649607.1:c.3359+136G>T
|
|
|
ENST00000649775.1:c.1664+136G>T
|
|
|
ENST00000650226.1:c.5175+136G>T
|
ENSP00000496981.1:n.5175+136G>T
|
|
ENST00000281928.7:c.5175+136G>T
|
ENSP00000281928.3:n.5175+136G>T
|
|
ENST00000549786.1:c.675G>T
|
|
|
ENST00000552340.1:c.207+136G>T
|
ENSP00000449876.1:n.207+136G>T
|
|
NM_015335.4:c.5175+136G>T
|
NP_056150.1:n.5175+136G>T
|
|
XM_011538080.1:c.5175+136G>T
|
XP_011536382.1:n.5175+136G>T
|
|
XM_011538081.1:c.5172+136G>T
|
XP_011536383.1:n.5172+136G>T
|
|
XM_011538082.1:c.5145+136G>T
|
XP_011536384.1:n.5145+136G>T
|
|
XM_011538080.2:c.5175+136G>T
|
XP_011536382.1:n.5175+136G>T
|
|
XM_011538081.2:c.5172+136G>T
|
XP_011536383.1:n.5172+136G>T
|
|
XM_011538082.2:c.5145+136G>T
|
XP_011536384.1:n.5145+136G>T
|
|
XM_017019090.1:c.5172+136G>T
|
XP_016874579.1:n.5172+136G>T
|
|
NM_015335.5:c.5175+136G>T
MANE Select
|
NP_056150.1:n.5175+136G>T
|
|