ENST00000703783.1:n.1068C>G
|
|
|
ENST00000703785.1:n.1149C>G
|
|
|
ENST00000262464.9:c.4284C>G
MANE Select
|
ENSP00000262464.4:p.Thr1428=
|
|
ENST00000262464.8:c.4284C>G
|
ENSP00000262464.4:p.Thr1428=
|
|
ENST00000507835.5:c.834C>G
|
ENSP00000426839.1:p.Thr278=
|
|
ENST00000508053.5:c.4284C>G
|
ENSP00000424571.1:p.Thr1428=
|
|
ENST00000508989.5:c.4185C>G
|
ENSP00000425596.1:p.Thr1395=
|
|
ENST00000619499.4:c.4281C>G
|
ENSP00000482132.1:p.Thr1427=
|
|
NM_001999.3:c.4284C>G
|
NP_001990.2:p.Thr1428=
|
|
XM_017009228.2:c.4131C>G
|
XP_016864717.1:p.Thr1377=
|
|
NM_001999.4:c.4284C>G
MANE Select
|
NP_001990.2:p.Thr1428=
|
|