ENST00000371270.6:c.1311A>C
MANE Select
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ENSP00000360317.3:p.Gly437=
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ENST00000371270.5:c.1311A>C
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ENSP00000360317.3:p.Gly437=
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ENST00000490994.6:c.*1097A>C
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ENSP00000433314.1:n.*1097A>C
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ENST00000525991.5:c.*886A>C
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ENSP00000433842.1:n.*886A>C
|
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ENST00000526814.5:n.1566A>C
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ENST00000527420.5:c.*168A>C
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ENSP00000433191.1:n.*168A>C
|
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ENST00000527953.5:n.1605A>C
|
|
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ENST00000531714.1:n.499A>C
|
|
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ENST00000533320.5:n.1545A>C
|
|
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ENST00000535898.5:c.1005A>C
|
ENSP00000445062.1:p.Gly335=
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ENST00000539050.5:c.1101A>C
|
ENSP00000442343.2:p.Gly367=
|
|
ENST00000623108.3:c.1101A>C
|
ENSP00000485110.1:p.Gly367=
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|
NM_000770.3:c.1311A>C
MANE Select
|
NP_000761.3:p.Gly437=
|
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NM_001198853.1:c.1101A>C
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NP_001185782.1:p.Gly367=
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NM_001198854.1:c.1005A>C
|
NP_001185783.1:p.Gly335=
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|
NM_001198855.1:c.1101A>C
|
NP_001185784.1:p.Gly367=
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XR_945610.1:n.1446A>C
|
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