ENST00000703783.1:n.721G>C
|
|
|
ENST00000703785.1:n.802G>C
|
|
|
ENST00000262464.9:c.3937G>C
MANE Select
|
ENSP00000262464.4:p.Gly1313Arg
|
|
ENST00000262464.8:c.3937G>C
|
ENSP00000262464.4:p.Gly1313Arg
|
|
ENST00000507835.5:c.487G>C
|
ENSP00000426839.1:p.Gly163Arg
|
|
ENST00000508053.5:c.3937G>C
|
ENSP00000424571.1:p.Gly1313Arg
|
|
ENST00000508989.5:c.3838G>C
|
ENSP00000425596.1:p.Gly1280Arg
|
|
ENST00000619499.4:c.3934G>C
|
ENSP00000482132.1:p.Gly1312Arg
|
|
NM_001999.3:c.3937G>C
|
NP_001990.2:p.Gly1313Arg
|
|
XM_017009228.2:c.3784G>C
|
XP_016864717.1:p.Gly1262Arg
|
|
NM_001999.4:c.3937G>C
MANE Select
|
NP_001990.2:p.Gly1313Arg
|
|