ENST00000460680.6:c.1988A>T
MANE Select
|
ENSP00000417132.1:p.Asp663Val
|
|
ENST00000296288.9:c.1934A>T
|
ENSP00000296288.5:p.Asp645Val
|
|
ENST00000460680.5:c.1988A>T
|
ENSP00000417132.1:p.Asp663Val
|
|
ENST00000466093.1:n.661A>T
|
|
|
ENST00000469613.5:c.187A>T
|
|
|
ENST00000478368.1:c.560A>T
|
ENSP00000420647.1:p.Asp187Val
|
|
NM_004656.3:c.1988A>T
|
NP_004647.1:p.Asp663Val
|
|
XM_011534149.1:c.2057A>T
|
XP_011532451.1:p.Asp686Val
|
|
XM_011534150.1:c.2012A>T
|
XP_011532452.1:p.Asp671Val
|
|
XM_011534151.1:c.2003A>T
|
XP_011532453.1:p.Asp668Val
|
|
XM_011534152.1:c.1943A>T
|
XP_011532454.1:p.Asp648Val
|
|
XM_011534149.3:c.2057A>T
|
XP_011532451.1:p.Asp686Val
|
|
XM_011534150.3:c.2012A>T
|
XP_011532452.1:p.Asp671Val
|
|
XM_011534151.3:c.2003A>T
|
XP_011532453.1:p.Asp668Val
|
|
XM_011534152.2:c.1943A>T
|
XP_011532454.1:p.Asp648Val
|
|
XM_017007303.2:c.1934A>T
|
XP_016862792.1:p.Asp645Val
|
|
NM_004656.4:c.1988A>T
MANE Select
|
NP_004647.1:p.Asp663Val
|
|