ENST00000703783.1:n.536G>C
|
|
|
ENST00000703785.1:n.617G>C
|
|
|
ENST00000262464.9:c.3752G>C
MANE Select
|
ENSP00000262464.4:p.Gly1251Ala
|
|
ENST00000262464.8:c.3752G>C
|
ENSP00000262464.4:p.Gly1251Ala
|
|
ENST00000507835.5:c.302G>C
|
ENSP00000426839.1:p.Gly101Ala
|
|
ENST00000508053.5:c.3752G>C
|
ENSP00000424571.1:p.Gly1251Ala
|
|
ENST00000508989.5:c.3653G>C
|
ENSP00000425596.1:p.Gly1218Ala
|
|
ENST00000619499.4:c.3749G>C
|
ENSP00000482132.1:p.Gly1250Ala
|
|
NM_001999.3:c.3752G>C
|
NP_001990.2:p.Gly1251Ala
|
|
XM_017009228.2:c.3599G>C
|
XP_016864717.1:p.Gly1200Ala
|
|
NM_001999.4:c.3752G>C
MANE Select
|
NP_001990.2:p.Gly1251Ala
|
|