ENST00000391944.8:c.1449G=
|
ENSP00000375808.4:p.Met483=
|
|
ENST00000682414.1:c.1449G=
|
ENSP00000507019.1:p.Met483=
|
|
ENST00000682508.1:n.1478G=
|
|
|
ENST00000684218.1:c.*707G=
|
ENSP00000507804.1:n.*707G=
|
|
ENST00000684264.1:n.1005G=
|
|
|
ENST00000684407.1:c.1326G=
|
ENSP00000507775.1:p.Met442=
|
|
ENST00000684458.1:c.1379G=
|
ENSP00000508260.1:p.Ter460=
|
|
ENST00000684468.1:n.1225G=
|
|
|
ENST00000391945.10:c.1449G=
MANE Select
|
ENSP00000375809.4:p.Met483=
|
|
ENST00000587376.6:c.572G=
|
|
|
ENST00000646507.1:n.1546G=
|
|
|
ENST00000391941.6:c.1377G=
|
ENSP00000375805.2:p.Met459=
|
|
ENST00000391942.6:n.620G=
|
|
|
ENST00000391944.7:c.1215G=
|
ENSP00000375808.3:p.Met405=
|
|
ENST00000391945.8:c.1449G=
|
ENSP00000375809.3:p.Met483=
|
|
ENST00000587376.5:c.572G=
|
|
|
ENST00000588652.5:n.1537G=
|
|
|
NM_000400.3:c.1449G= , LRG_461t1:c.1449G=
|
NP_000391.1:p.Met483=
|
|
XM_011526611.1:c.1371G=
|
XP_011524913.1:p.Met457=
|
|
XR_935763.1:n.1496G=
|
|
|
XM_011526611.2:c.1371G=
|
XP_011524913.1:p.Met457=
|
|
XM_017026467.1:c.1326G=
|
XP_016881956.1:p.Met442=
|
|
XR_001753633.2:n.1496G=
|
|
|
XR_001753634.2:n.1496G=
|
|
|
NM_000400.4:c.1449G=
MANE Select
|
NP_000391.1:p.Met483=
|
|