ENST00000394975.3:c.449T>G
MANE Select
|
ENSP00000378426.2:p.Phe150Cys
|
|
ENST00000300851.10:c.*60T>G
|
ENSP00000300851.6:n.*60T>G
|
|
ENST00000319788.11:c.*60T>G
|
ENSP00000326135.7:n.*60T>G
|
|
ENST00000354895.4:c.*60T>G
|
ENSP00000346969.4:n.*60T>G
|
|
ENST00000394971.7:c.*60T>G
|
ENSP00000378422.3:n.*60T>G
|
|
ENST00000394975.2:c.449T>G
|
ENSP00000378426.2:p.Phe150Cys
|
|
ENST00000420057.2:c.411T>G
|
|
|
ENST00000498155.1:c.*60T>G
|
ENSP00000417662.1:n.*60T>G
|
|
ENST00000529564.1:c.283+2135T>G
|
ENSP00000431371.1:n.283+2135T>G
|
|
ENST00000532364.1:c.173+3380T>G
|
ENSP00000460316.1:n.173+3380T>G
|
|
ENST00000533518.5:c.322T>G
|
|
|
NM_001311311.1:c.533T>G
|
NP_001298240.1:p.Phe178Cys
|
|
NM_024006.4:c.449T>G
|
NP_076869.1:p.Phe150Cys
|
|
NM_024006.5:c.449T>G
|
NP_076869.1:p.Phe150Cys
|
|
NM_206824.1:c.*60T>G
|
NP_996560.1:n.*60T>G
|
|
NM_206824.2:c.*60T>G
|
NP_996560.1:n.*60T>G
|
|
XM_011545944.1:c.449T>G
|
XP_011544246.1:p.Phe150Cys
|
|
XM_011545945.1:c.*60T>G
|
XP_011544247.1:n.*60T>G
|
|
XR_950848.1:n.1237T>G
|
|
|
NM_024006.6:c.449T>G
MANE Select
|
NP_076869.1:p.Phe150Cys
|
|
NM_001311311.2:c.533T>G
|
NP_001298240.1:p.Phe178Cys
|
|
NM_206824.3:c.*60T>G
|
NP_996560.1:n.*60T>G
|
|