ENST00000455537.7:c.874C>T
MANE Select
|
ENSP00000408979.2:p.Leu292Phe
|
|
ENST00000674619.1:c.874C>T
|
ENSP00000502270.1:p.Leu292Phe
|
|
ENST00000676081.1:n.20C>T
|
|
|
ENST00000676457.1:c.769C>T
|
ENSP00000501588.1:p.Leu257Phe
|
|
ENST00000286452.5:c.607C>T
|
ENSP00000286452.5:p.Leu203Phe
|
|
ENST00000455537.6:c.874C>T
|
ENSP00000408979.2:p.Leu292Phe
|
|
NM_004984.2:c.874C>T
|
NP_004975.2:p.Leu292Phe
|
|
NM_001354705.1:c.607C>T
|
NP_001341634.1:p.Leu203Phe
|
|
NM_004984.3:c.874C>T
|
NP_004975.2:p.Leu292Phe
|
|
XR_002957324.1:n.1107C>T
|
|
|
NM_004984.4:c.874C>T
MANE Select
|
NP_004975.2:p.Leu292Phe
|
|
NM_001354705.2:c.607C>T
|
NP_001341634.1:p.Leu203Phe
|
|