ENST00000463045.3:c.346T=
|
ENSP00000481376.2:p.Ser116=
|
|
ENST00000491274.6:c.475T=
|
ENSP00000480482.2:p.Ser159=
|
|
ENST00000375499.8:c.517T=
MANE Select
|
ENSP00000364649.3:p.Ser173=
|
|
ENST00000375499.7:c.517T=
|
ENSP00000364649.3:p.Ser173=
|
|
ENST00000463045.2:c.346T=
|
ENSP00000481376.1:p.Ser116=
|
|
ENST00000475506.1:n.434T=
|
|
|
ENST00000485515.5:n.451T=
|
|
|
ENST00000491274.5:c.475T=
|
ENSP00000480482.1:p.Ser159=
|
|
NM_003000.2:c.517T= , LRG_316t1:c.517T=
|
NP_002991.2:p.Ser173=
|
|
NM_003000.3:c.517T=
MANE Select
|
NP_002991.2:p.Ser173=
|
|