ENST00000389039.11:c.2654+148T>A
MANE Select
|
ENSP00000373691.7:n.2654+148T>A
|
|
ENST00000389039.10:c.2654+148T>A
|
ENSP00000373691.6:n.2654+148T>A
|
|
ENST00000558383.1:n.4385+148T>A
|
|
|
ENST00000603300.1:c.2654+148T>A
|
ENSP00000475084.1:n.2654+148T>A
|
|
NM_014080.4:c.2654+148T>A
|
NP_054799.4:n.2654+148T>A
|
|
XM_005254421.2:c.2654+148T>A
|
XP_005254478.1:n.2654+148T>A
|
|
NM_001363711.1:c.2654+148T>A
|
NP_001350640.1:n.2654+148T>A
|
|
NM_001363711.2:c.2654+148T>A
MANE Select
|
NP_001350640.1:n.2654+148T>A
|
|
NM_014080.5:c.2654+148T>A
|
NP_054799.4:n.2654+148T>A
|
|