ENST00000703783.1:n.723C>T
|
|
|
ENST00000703785.1:n.804C>T
|
|
|
ENST00000262464.9:c.3939C>T
MANE Select
|
ENSP00000262464.4:p.Gly1313=
|
|
ENST00000262464.8:c.3939C>T
|
ENSP00000262464.4:p.Gly1313=
|
|
ENST00000507835.5:c.489C>T
|
ENSP00000426839.1:p.Gly163=
|
|
ENST00000508053.5:c.3939C>T
|
ENSP00000424571.1:p.Gly1313=
|
|
ENST00000508989.5:c.3840C>T
|
ENSP00000425596.1:p.Gly1280=
|
|
ENST00000619499.4:c.3936C>T
|
ENSP00000482132.1:p.Gly1312=
|
|
NM_001999.3:c.3939C>T
|
NP_001990.2:p.Gly1313=
|
|
XM_017009228.2:c.3786C>T
|
XP_016864717.1:p.Gly1262=
|
|
NM_001999.4:c.3939C>T
MANE Select
|
NP_001990.2:p.Gly1313=
|
|