ENST00000262494.13:c.621T>A
|
ENSP00000262494.7:p.Ser207=
|
|
ENST00000262493.12:c.621T>A
MANE Select
|
ENSP00000262493.6:p.Ser207=
|
|
ENST00000262494.12:c.621T>A
|
ENSP00000262494.7:p.Ser207=
|
|
ENST00000562316.6:c.288T>A
|
ENSP00000457238.2:p.Ser96=
|
|
ENST00000568375.2:c.13T>A
|
|
|
ENST00000638185.1:n.836T>A
|
|
|
ENST00000638210.1:n.921T>A
|
|
|
ENST00000638705.1:c.621T>A
|
ENSP00000491223.1:p.Ser207=
|
|
ENST00000638836.1:n.531T>A
|
|
|
ENST00000639055.1:n.1342T>A
|
|
|
ENST00000639251.1:n.522T>A
|
|
|
ENST00000639268.1:c.256T>A
|
|
|
ENST00000639341.1:c.146T>A
|
|
|
ENST00000639770.1:c.659T>A
|
ENSP00000491999.1:n.659T>A
|
|
ENST00000640390.1:n.551T>A
|
|
|
ENST00000640560.1:n.397T>A
|
|
|
ENST00000640893.1:c.*19T>A
|
ENSP00000492677.1:n.*19T>A
|
|
ENST00000262493.10:c.621T>A
|
ENSP00000262493.6:p.Ser207=
|
|
ENST00000262494.11:c.621T>A
|
ENSP00000262494.7:p.Ser207=
|
|
ENST00000568375.1:n.13T>A
|
|
|
NM_020988.2:c.621T>A
|
NP_066268.1:p.Ser207=
|
|
NM_138736.2:c.621T>A
|
NP_620073.2:p.Ser207=
|
|
XM_011523003.1:c.495T>A
|
XP_011521305.1:p.Ser165=
|
|
XM_011523003.3:c.495T>A
|
XP_011521305.1:p.Ser165=
|
|
NM_020988.3:c.621T>A
MANE Select
|
NP_066268.1:p.Ser207=
|
|
NM_138736.3:c.621T>A
|
NP_620073.2:p.Ser207=
|
|