ENST00000703783.1:n.1099G>C
|
|
|
ENST00000703785.1:n.1180G>C
|
|
|
ENST00000262464.9:c.4315G>C
MANE Select
|
ENSP00000262464.4:p.Gly1439Arg
|
|
ENST00000262464.8:c.4315G>C
|
ENSP00000262464.4:p.Gly1439Arg
|
|
ENST00000507835.5:c.865G>C
|
ENSP00000426839.1:p.Gly289Arg
|
|
ENST00000508053.5:c.4315G>C
|
ENSP00000424571.1:p.Gly1439Arg
|
|
ENST00000508989.5:c.4216G>C
|
ENSP00000425596.1:p.Gly1406Arg
|
|
ENST00000619499.4:c.4312G>C
|
ENSP00000482132.1:p.Gly1438Arg
|
|
NM_001999.3:c.4315G>C
|
NP_001990.2:p.Gly1439Arg
|
|
XM_017009228.2:c.4162G>C
|
XP_016864717.1:p.Gly1388Arg
|
|
NM_001999.4:c.4315G>C
MANE Select
|
NP_001990.2:p.Gly1439Arg
|
|