ENST00000371270.6:c.1362G>T
MANE Select
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ENSP00000360317.3:p.Gln454His
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ENST00000371270.5:c.1362G>T
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ENSP00000360317.3:p.Gln454His
|
|
ENST00000490994.6:c.*1148G>T
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ENSP00000433314.1:n.*1148G>T
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ENST00000525991.5:c.*937G>T
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ENSP00000433842.1:n.*937G>T
|
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ENST00000526814.5:n.1617G>T
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|
|
ENST00000527420.5:c.*219G>T
|
ENSP00000433191.1:n.*219G>T
|
|
ENST00000527953.5:n.1656G>T
|
|
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ENST00000531714.1:n.550G>T
|
|
|
ENST00000533320.5:n.1596G>T
|
|
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ENST00000535898.5:c.1056G>T
|
ENSP00000445062.1:p.Gln352His
|
|
ENST00000539050.5:c.1152G>T
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ENSP00000442343.2:p.Gln384His
|
|
ENST00000623108.3:c.1152G>T
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ENSP00000485110.1:p.Gln384His
|
|
NM_000770.3:c.1362G>T
MANE Select
|
NP_000761.3:p.Gln454His
|
|
NM_001198853.1:c.1152G>T
|
NP_001185782.1:p.Gln384His
|
|
NM_001198854.1:c.1056G>T
|
NP_001185783.1:p.Gln352His
|
|
NM_001198855.1:c.1152G>T
|
NP_001185784.1:p.Gln384His
|
|
XR_945610.1:n.1497G>T
|
|
|