ENST00000460680.6:c.2118C>A
MANE Select
|
ENSP00000417132.1:p.Ile706=
|
|
ENST00000296288.9:c.2064C>A
|
ENSP00000296288.5:p.Ile688=
|
|
ENST00000460680.5:c.2118C>A
|
ENSP00000417132.1:p.Ile706=
|
|
ENST00000466093.1:n.791C>A
|
|
|
ENST00000469613.5:c.317C>A
|
|
|
ENST00000478368.1:c.690C>A
|
ENSP00000420647.1:p.Ile230=
|
|
NM_004656.3:c.2118C>A
|
NP_004647.1:p.Ile706=
|
|
XM_011534149.1:c.2187C>A
|
XP_011532451.1:p.Ile729=
|
|
XM_011534150.1:c.2142C>A
|
XP_011532452.1:p.Ile714=
|
|
XM_011534151.1:c.2133C>A
|
XP_011532453.1:p.Ile711=
|
|
XM_011534152.1:c.2073C>A
|
XP_011532454.1:p.Ile691=
|
|
XM_011534149.3:c.2187C>A
|
XP_011532451.1:p.Ile729=
|
|
XM_011534150.3:c.2142C>A
|
XP_011532452.1:p.Ile714=
|
|
XM_011534151.3:c.2133C>A
|
XP_011532453.1:p.Ile711=
|
|
XM_011534152.2:c.2073C>A
|
XP_011532454.1:p.Ile691=
|
|
XM_017007303.2:c.2064C>A
|
XP_016862792.1:p.Ile688=
|
|
NM_004656.4:c.2118C>A
MANE Select
|
NP_004647.1:p.Ile706=
|
|