ENST00000262493.12:c.761T>G
MANE Select
|
ENSP00000262493.6:p.Ile254Ser
|
|
ENST00000562316.6:c.428T>G
|
ENSP00000457238.2:p.Ile143Ser
|
|
ENST00000564727.2:c.65T>G
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ENSP00000454971.2:p.Ile22Ser
|
|
ENST00000568375.2:c.116-3445T>G
|
|
|
ENST00000638185.1:n.976T>G
|
|
|
ENST00000638210.1:n.1061T>G
|
|
|
ENST00000638705.1:c.761T>G
|
ENSP00000491223.1:p.Ile254Ser
|
|
ENST00000638836.1:n.671T>G
|
|
|
ENST00000639055.1:n.1482T>G
|
|
|
ENST00000639251.1:n.662T>G
|
|
|
ENST00000639268.1:c.396T>G
|
|
|
ENST00000639341.1:c.286T>G
|
|
|
ENST00000639770.1:c.799T>G
|
ENSP00000491999.1:n.799T>G
|
|
ENST00000640390.1:n.691T>G
|
|
|
ENST00000640469.1:c.125T>G
|
ENSP00000491875.1:p.Ile42Ser
|
|
ENST00000640560.1:n.537T>G
|
|
|
ENST00000640893.1:c.*159T>G
|
ENSP00000492677.1:n.*159T>G
|
|
ENST00000262493.10:c.761T>G
|
ENSP00000262493.6:p.Ile254Ser
|
|
ENST00000568375.1:n.116-3445T>G
|
|
|
NM_020988.2:c.761T>G
|
NP_066268.1:p.Ile254Ser
|
|
XM_011523003.1:c.635T>G
|
XP_011521305.1:p.Ile212Ser
|
|
XM_011523003.3:c.635T>G
|
XP_011521305.1:p.Ile212Ser
|
|
NM_020988.3:c.761T>G
MANE Select
|
NP_066268.1:p.Ile254Ser
|
|