ENST00000379727.8:c.1420C>T
MANE Select
|
ENSP00000369050.3:p.Leu474=
|
|
ENST00000379727.7:c.1420C>T
|
ENSP00000369050.3:p.Leu474=
|
|
ENST00000395048.6:c.1420C>T
|
ENSP00000378488.2:p.Leu474=
|
|
ENST00000395049.8:c.1333C>T
|
ENSP00000378489.4:p.Leu445=
|
|
ENST00000567032.5:c.1420C>T
|
ENSP00000456585.1:p.Leu474=
|
|
ENST00000612821.4:c.1336C>T
|
ENSP00000479744.1:p.Leu446=
|
|
ENST00000617691.4:c.1333C>T
|
ENSP00000482863.1:p.Leu445=
|
|
NM_000499.3:c.1420C>T
|
NP_000490.1:p.Leu474=
|
|
XM_005254185.1:c.1420C>T
|
XP_005254242.1:p.Leu474=
|
|
NM_000499.5:c.1420C>T
|
NP_000490.1:p.Leu474=
|
|
NM_001319216.2:c.1333C>T
|
NP_001306145.1:p.Leu445=
|
|
NM_001319217.2:c.1420C>T
MANE Select
|
NP_001306146.1:p.Leu474=
|
|