ENST00000262493.12:c.737A=
MANE Select
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ENSP00000262493.6:p.Glu246=
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ENST00000562316.6:c.404A=
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ENSP00000457238.2:p.Glu135=
|
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ENST00000564727.2:c.41A=
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ENSP00000454971.2:p.Glu14=
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ENST00000568375.2:c.116-3469A=
|
|
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ENST00000638185.1:n.952A=
|
|
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ENST00000638210.1:n.1037A=
|
|
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ENST00000638705.1:c.737A=
|
ENSP00000491223.1:p.Glu246=
|
|
ENST00000638836.1:n.647A=
|
|
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ENST00000639055.1:n.1458A=
|
|
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ENST00000639251.1:n.638A=
|
|
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ENST00000639268.1:c.372A=
|
|
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ENST00000639341.1:c.262A=
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|
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ENST00000639770.1:c.775A=
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ENSP00000491999.1:n.775A=
|
|
ENST00000640390.1:n.667A=
|
|
|
ENST00000640469.1:c.101A=
|
ENSP00000491875.1:p.Glu34=
|
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ENST00000640560.1:n.513A=
|
|
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ENST00000640893.1:c.*135A=
|
ENSP00000492677.1:n.*135A=
|
|
ENST00000262493.10:c.737A=
|
ENSP00000262493.6:p.Glu246=
|
|
ENST00000568375.1:n.116-3469A=
|
|
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NM_020988.2:c.737A=
|
NP_066268.1:p.Glu246=
|
|
XM_011523003.1:c.611A=
|
XP_011521305.1:p.Glu204=
|
|
XM_011523003.3:c.611A=
|
XP_011521305.1:p.Glu204=
|
|
NM_020988.3:c.737A=
MANE Select
|
NP_066268.1:p.Glu246=
|
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