ENST00000703783.1:n.357G>T
|
|
|
ENST00000703785.1:n.438G>T
|
|
|
ENST00000262464.9:c.3573G>T
MANE Select
|
ENSP00000262464.4:p.Leu1191=
|
|
ENST00000262464.8:c.3573G>T
|
ENSP00000262464.4:p.Leu1191=
|
|
ENST00000507835.5:c.123G>T
|
ENSP00000426839.1:p.Leu41=
|
|
ENST00000508053.5:c.3573G>T
|
ENSP00000424571.1:p.Leu1191=
|
|
ENST00000508989.5:c.3474G>T
|
ENSP00000425596.1:p.Leu1158=
|
|
ENST00000619499.4:c.3570G>T
|
ENSP00000482132.1:p.Leu1190=
|
|
NM_001999.3:c.3573G>T
|
NP_001990.2:p.Leu1191=
|
|
XM_017009228.2:c.3420G>T
|
XP_016864717.1:p.Leu1140=
|
|
NM_001999.4:c.3573G>T
MANE Select
|
NP_001990.2:p.Leu1191=
|
|