ENST00000360124.10:c.711G=
|
ENSP00000353241.6:p.Leu237=
|
|
ENST00000645361.2:c.913G=
MANE Select
|
ENSP00000496150.1:p.Ala305=
|
|
ENST00000359033.4:c.760G=
|
ENSP00000351927.4:p.Ala254=
|
|
ENST00000360124.9:c.531G=
|
ENSP00000353241.5:p.Leu177=
|
|
ENST00000360608.9:c.913G=
|
ENSP00000353820.5:p.Ala305=
|
|
ENST00000389970.7:c.847G=
|
ENSP00000374620.4:p.Ala283=
|
|
ENST00000488442.1:n.1637G=
|
|
|
NM_000106.5:c.913G=
|
NP_000097.3:p.Ala305=
|
|
NM_001025161.2:c.760G=
|
NP_001020332.2:p.Ala254=
|
|
XM_011529966.1:c.913G=
|
XP_011528268.1:p.Ala305=
|
|
XM_011529967.1:c.913G=
|
XP_011528269.1:p.Ala305=
|
|
XM_011529968.1:c.913G=
|
XP_011528270.1:p.Ala305=
|
|
XM_011529969.1:c.769G=
|
XP_011528271.1:p.Ala257=
|
|
XM_011529970.1:c.760G=
|
XP_011528272.1:p.Ala254=
|
|
XM_011529971.1:c.769G=
|
XP_011528273.1:p.Ala257=
|
|
XM_011529972.1:c.843+260G=
|
XP_011528274.1:n.843+260G=
|
|
NM_000106.6:c.913G=
MANE Select
|
NP_000097.3:p.Ala305=
|
|
NM_001025161.3:c.760G=
|
NP_001020332.2:p.Ala254=
|
|