ENST00000642496.1:c.4034T>G
|
|
|
ENST00000644397.2:c.5175T>G
MANE Select
|
ENSP00000495195.1:p.Leu1725=
|
|
ENST00000373965.6:c.4986T>G
|
ENSP00000363076.3:p.Leu1662=
|
|
ENST00000414778.5:c.4983T>G
|
ENSP00000410304.2:p.Leu1661=
|
|
ENST00000495484.5:c.1203T>G
|
ENSP00000480780.1:p.Leu401=
|
|
ENST00000614895.4:c.4998T>G
|
ENSP00000478512.1:p.Leu1666=
|
|
ENST00000616114.4:c.4980T>G
|
ENSP00000483745.1:p.Leu1660=
|
|
ENST00000618301.4:c.1335T>G
|
ENSP00000482780.1:p.Leu445=
|
|
ENST00000621708.4:c.5001T>G
|
ENSP00000484454.1:p.Leu1667=
|
|
NM_001142771.1:c.5001T>G
|
NP_001136243.1:p.Leu1667=
|
|
NM_001142772.1:c.4986T>G
|
NP_001136244.1:p.Leu1662=
|
|
NM_001354420.1:c.4980T>G
|
NP_001341349.1:p.Leu1660=
|
|
NM_001354429.1:c.5109T>G
|
NP_001341358.1:p.Leu1703=
|
|
XR_001747192.2:n.11467T>G
|
|
|
XR_001747193.2:n.11458T>G
|
|
|
NM_001142771.2:c.5001T>G
|
NP_001136243.1:p.Leu1667=
|
|
NM_001142772.2:c.4986T>G
|
NP_001136244.1:p.Leu1662=
|
|
NM_001354420.2:c.4980T>G
|
NP_001341349.1:p.Leu1660=
|
|
NM_001354429.2:c.5109T>G
|
NP_001341358.1:p.Leu1703=
|
|
NM_001384140.1:c.5175T>G
MANE Select
|
NP_001371069.1:p.Leu1725=
|
|