ENST00000703783.1:n.1011G=
|
|
|
ENST00000703785.1:n.1092G=
|
|
|
ENST00000262464.9:c.4227G=
MANE Select
|
ENSP00000262464.4:p.Leu1409=
|
|
ENST00000262464.8:c.4227G=
|
ENSP00000262464.4:p.Leu1409=
|
|
ENST00000507835.5:c.777G=
|
ENSP00000426839.1:p.Leu259=
|
|
ENST00000508053.5:c.4227G=
|
ENSP00000424571.1:p.Leu1409=
|
|
ENST00000508989.5:c.4128G=
|
ENSP00000425596.1:p.Leu1376=
|
|
ENST00000619499.4:c.4224G=
|
ENSP00000482132.1:p.Leu1408=
|
|
NM_001999.3:c.4227G=
|
NP_001990.2:p.Leu1409=
|
|
XM_017009228.2:c.4074G=
|
XP_016864717.1:p.Leu1358=
|
|
NM_001999.4:c.4227G=
MANE Select
|
NP_001990.2:p.Leu1409=
|
|