ENST00000460680.6:c.2020T>G
MANE Select
|
ENSP00000417132.1:p.Phe674Val
|
|
ENST00000296288.9:c.1966T>G
|
ENSP00000296288.5:p.Phe656Val
|
|
ENST00000460680.5:c.2020T>G
|
ENSP00000417132.1:p.Phe674Val
|
|
ENST00000466093.1:n.693T>G
|
|
|
ENST00000469613.5:c.219T>G
|
|
|
ENST00000478368.1:c.592T>G
|
ENSP00000420647.1:p.Phe198Val
|
|
NM_004656.3:c.2020T>G
|
NP_004647.1:p.Phe674Val
|
|
XM_011534149.1:c.2089T>G
|
XP_011532451.1:p.Phe697Val
|
|
XM_011534150.1:c.2044T>G
|
XP_011532452.1:p.Phe682Val
|
|
XM_011534151.1:c.2035T>G
|
XP_011532453.1:p.Phe679Val
|
|
XM_011534152.1:c.1975T>G
|
XP_011532454.1:p.Phe659Val
|
|
XM_011534149.3:c.2089T>G
|
XP_011532451.1:p.Phe697Val
|
|
XM_011534150.3:c.2044T>G
|
XP_011532452.1:p.Phe682Val
|
|
XM_011534151.3:c.2035T>G
|
XP_011532453.1:p.Phe679Val
|
|
XM_011534152.2:c.1975T>G
|
XP_011532454.1:p.Phe659Val
|
|
XM_017007303.2:c.1966T>G
|
XP_016862792.1:p.Phe656Val
|
|
NM_004656.4:c.2020T>G
MANE Select
|
NP_004647.1:p.Phe674Val
|
|