ENST00000281928.9:c.5175+229T>C
MANE Select
|
ENSP00000281928.3:n.5175+229T>C
|
|
ENST00000549786.2:c.4832T>C
|
|
|
ENST00000648379.1:n.3543+229T>C
|
|
|
ENST00000648737.1:n.4939+229T>C
|
|
|
ENST00000648825.1:n.2144T>C
|
|
|
ENST00000648916.1:n.3186+229T>C
|
|
|
ENST00000649146.1:n.2647T>C
|
|
|
ENST00000649607.1:c.3359+229T>C
|
|
|
ENST00000649775.1:c.1664+229T>C
|
|
|
ENST00000650226.1:c.5175+229T>C
|
ENSP00000496981.1:n.5175+229T>C
|
|
ENST00000281928.7:c.5175+229T>C
|
ENSP00000281928.3:n.5175+229T>C
|
|
ENST00000549786.1:c.768T>C
|
|
|
ENST00000552340.1:c.207+229T>C
|
ENSP00000449876.1:n.207+229T>C
|
|
NM_015335.4:c.5175+229T>C
|
NP_056150.1:n.5175+229T>C
|
|
XM_011538080.1:c.5175+229T>C
|
XP_011536382.1:n.5175+229T>C
|
|
XM_011538081.1:c.5172+229T>C
|
XP_011536383.1:n.5172+229T>C
|
|
XM_011538082.1:c.5145+229T>C
|
XP_011536384.1:n.5145+229T>C
|
|
XM_011538080.2:c.5175+229T>C
|
XP_011536382.1:n.5175+229T>C
|
|
XM_011538081.2:c.5172+229T>C
|
XP_011536383.1:n.5172+229T>C
|
|
XM_011538082.2:c.5145+229T>C
|
XP_011536384.1:n.5145+229T>C
|
|
XM_017019090.1:c.5172+229T>C
|
XP_016874579.1:n.5172+229T>C
|
|
NM_015335.5:c.5175+229T>C
MANE Select
|
NP_056150.1:n.5175+229T>C
|
|