ENST00000704074.1:c.275G>T
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|
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ENST00000283179.14:c.597G>T
|
ENSP00000283179.10:p.Ala199=
|
|
ENST00000444376.7:c.597G>T
|
ENSP00000393151.2:p.Ala199=
|
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ENST00000476241.2:n.782G>T
|
|
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ENST00000638475.1:c.381G>T
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ENSP00000491305.1:p.Ala127=
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ENST00000638952.1:n.828G>T
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|
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ENST00000640218.2:c.597G>T
MANE Select
|
ENSP00000491215.1:p.Ala199=
|
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ENST00000640306.1:c.597G>T
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ENSP00000491685.1:p.Ala199=
|
|
ENST00000640440.1:c.297G>T
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ENSP00000491263.1:p.Ala99=
|
|
ENST00000649899.1:n.821G>T
|
|
|
ENST00000283179.13:c.597G>T
|
ENSP00000283179.9:p.Ala199=
|
|
ENST00000444376.6:c.597G>T
|
ENSP00000393151.2:p.Ala199=
|
|
ENST00000476241.1:n.781G>T
|
|
|
NM_004501.3:c.597G>T
|
NP_004492.2:p.Ala199=
|
|
NM_031844.2:c.597G>T
|
NP_114032.2:p.Ala199=
|
|
NM_031844.3:c.597G>T
MANE Select
|
NP_114032.2:p.Ala199=
|
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