ENST00000223051.8:c.2061G>A
MANE Select
|
ENSP00000223051.3:p.Lys687=
|
|
ENST00000223051.7:c.2061G>A
|
ENSP00000223051.3:p.Lys687=
|
|
ENST00000431692.5:c.*736G>A
|
ENSP00000413905.1:n.*736G>A
|
|
ENST00000461176.1:n.407G>A
|
|
|
ENST00000462090.5:n.1097G>A
|
|
|
ENST00000462107.1:c.2061G>A
|
ENSP00000420525.1:p.Lys687=
|
|
ENST00000465294.5:n.1981G>A
|
|
|
ENST00000476304.5:n.1682G>A
|
|
|
ENST00000490084.5:c.1414G>A
|
|
|
NM_001206855.1:c.1548G>A
|
NP_001193784.1:p.Lys516=
|
|
NM_003227.3:c.2061G>A
|
NP_003218.2:p.Lys687=
|
|
XM_005250553.3:c.2061G>A
|
XP_005250610.1:p.Lys687=
|
|
XM_005250554.3:c.2061G>A
|
XP_005250611.1:p.Lys687=
|
|
XR_927814.1:n.433+4284C>T
|
|
|
NM_001206855.2:c.1548G>A
|
NP_001193784.1:p.Lys516=
|
|
XM_005250553.4:c.2061G>A
|
XP_005250610.1:p.Lys687=
|
|
XM_017012573.1:c.2061G>A
|
XP_016868062.1:p.Lys687=
|
|
NM_003227.4:c.2061G>A
MANE Select
|
NP_003218.2:p.Lys687=
|
|
NM_001206855.3:c.1548G>A
|
NP_001193784.1:p.Lys516=
|
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