ENST00000394975.3:c.*239G>T
MANE Select
|
ENSP00000378426.2:n.*239G>T
|
|
ENST00000300851.10:c.*342G>T
|
ENSP00000300851.6:n.*342G>T
|
|
ENST00000319788.11:c.*342G>T
|
ENSP00000326135.7:n.*342G>T
|
|
ENST00000354895.4:c.*342G>T
|
ENSP00000346969.4:n.*342G>T
|
|
ENST00000394975.2:c.*239G>T
|
ENSP00000378426.2:n.*239G>T
|
|
ENST00000420057.2:c.693G>T
|
|
|
ENST00000529564.1:c.283+2417G>T
|
ENSP00000431371.1:n.283+2417G>T
|
|
ENST00000532364.1:c.173+3662G>T
|
ENSP00000460316.1:n.173+3662G>T
|
|
ENST00000533518.5:c.407+197G>T
|
|
|
NM_001311311.1:c.*239G>T
|
NP_001298240.1:n.*239G>T
|
|
NM_024006.4:c.*239G>T
|
NP_076869.1:n.*239G>T
|
|
NM_024006.5:c.*239G>T
|
NP_076869.1:n.*239G>T
|
|
NM_206824.1:c.*342G>T
|
NP_996560.1:n.*342G>T
|
|
NM_206824.2:c.*342G>T
|
NP_996560.1:n.*342G>T
|
|
XM_011545944.1:c.*239G>T
|
XP_011544246.1:n.*239G>T
|
|
XM_011545945.1:c.*342G>T
|
XP_011544247.1:n.*342G>T
|
|
XR_950848.1:n.1519G>T
|
|
|
NM_024006.6:c.*239G>T
MANE Select
|
NP_076869.1:n.*239G>T
|
|
NM_001311311.2:c.*239G>T
|
NP_001298240.1:n.*239G>T
|
|
NM_206824.3:c.*342G>T
|
NP_996560.1:n.*342G>T
|
|