ENST00000281928.9:c.2610T>C
MANE Select
|
ENSP00000281928.3:p.Ser870=
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|
ENST00000548743.2:c.2580T>C
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ENSP00000448553.2:p.Ser860=
|
|
ENST00000549786.2:c.2038T>C
|
|
|
ENST00000647927.1:n.2983T>C
|
|
|
ENST00000648173.1:n.1405T>C
|
|
|
ENST00000648379.1:n.978T>C
|
|
|
ENST00000648737.1:n.2374T>C
|
|
|
ENST00000648916.1:n.621T>C
|
|
|
ENST00000649607.1:c.794T>C
|
|
|
ENST00000650226.1:c.2610T>C
|
ENSP00000496981.1:p.Ser870=
|
|
ENST00000281928.7:c.2610T>C
|
ENSP00000281928.3:p.Ser870=
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|
NM_015335.4:c.2610T>C
|
NP_056150.1:p.Ser870=
|
|
XM_011538080.1:c.2610T>C
|
XP_011536382.1:p.Ser870=
|
|
XM_011538081.1:c.2607T>C
|
XP_011536383.1:p.Ser869=
|
|
XM_011538082.1:c.2580T>C
|
XP_011536384.1:p.Ser860=
|
|
XM_011538080.2:c.2610T>C
|
XP_011536382.1:p.Ser870=
|
|
XM_011538081.2:c.2607T>C
|
XP_011536383.1:p.Ser869=
|
|
XM_011538082.2:c.2580T>C
|
XP_011536384.1:p.Ser860=
|
|
XM_017019090.1:c.2607T>C
|
XP_016874579.1:p.Ser869=
|
|
NM_015335.5:c.2610T>C
MANE Select
|
NP_056150.1:p.Ser870=
|
|