ENST00000254108.12:c.1564A=
MANE Select
|
ENSP00000254108.8:p.Arg522=
|
|
ENST00000254108.11:c.1564A=
|
ENSP00000254108.7:p.Arg522=
|
|
ENST00000380244.7:c.1561A=
|
ENSP00000369594.3:p.Arg521=
|
|
ENST00000483853.1:n.641A=
|
|
|
ENST00000487509.6:n.4739A=
|
|
|
ENST00000566605.5:c.*737A=
|
ENSP00000455073.1:n.*737A=
|
|
ENST00000568685.1:c.1567A=
|
ENSP00000455282.1:p.Arg523=
|
|
ENST00000569760.5:n.455A=
|
|
|
NM_001170634.1:c.1561A=
|
NP_001164105.1:p.Arg521=
|
|
NM_001170937.1:c.1552A=
|
NP_001164408.1:p.Arg518=
|
|
NM_004960.3:c.1564A= , LRG_655t1:c.1564A=
|
NP_004951.1:p.Arg522=
|
|
NR_028388.2:n.1634A=
|
|
|
XM_005255233.3:c.949A=
|
XP_005255290.1:p.Arg317=
|
|
XM_011545781.1:c.1558A=
|
XP_011544083.1:p.Arg520=
|
|
XM_011545782.1:c.949A=
|
XP_011544084.1:p.Arg317=
|
|
XM_005255233.5:c.949A=
|
XP_005255290.1:p.Arg317=
|
|
XM_011545782.2:c.949A=
|
XP_011544084.1:p.Arg317=
|
|
XM_024450221.1:c.1555A=
|
XP_024305989.1:p.Arg519=
|
|
NM_004960.4:c.1564A=
MANE Select
|
NP_004951.1:p.Arg522=
|
|