ENST00000356487.11:c.1576G>T
MANE Select
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ENSP00000348877.3:p.Glu526Ter
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ENST00000415930.8:c.1693G>T
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ENSP00000405573.3:p.Glu565Ter
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ENST00000586425.2:c.1242G>T
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|
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ENST00000588991.7:c.1609G>T
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ENSP00000465858.3:p.Glu537Ter
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ENST00000643067.1:n.2621G>T
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ENST00000647446.1:c.*627G>T
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ENSP00000495129.1:n.*627G>T
|
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ENST00000356487.9:c.1576G>T
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ENSP00000348877.3:p.Glu526Ter
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ENST00000415930.7:c.1609G>T
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ENSP00000405573.2:p.Glu537Ter
|
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ENST00000586077.1:n.2653G>T
|
|
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ENST00000586392.1:n.1314G>T
|
|
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ENST00000586425.1:c.*8G>T
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ENSP00000467670.2:n.*8G>T
|
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ENST00000588991.6:c.1621G>T
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ENSP00000465858.2:p.Glu541Ter
|
|
ENST00000592740.5:c.193+3278G>T
|
|
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NM_000175.3:c.1576G>T
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NP_000166.2:p.Glu526Ter
|
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NM_001184722.1:c.1609G>T
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NP_001171651.1:p.Glu537Ter
|
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NM_001289789.1:c.1693G>T
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NP_001276718.1:p.Glu565Ter
|
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NM_001289790.1:c.1492G>T
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NP_001276719.1:p.Glu498Ter
|
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XM_005258764.1:c.1576G>T
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XP_005258821.1:p.Glu526Ter
|
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XM_006723148.1:c.1576G>T
|
XP_006723211.1:p.Glu526Ter
|
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XM_011526754.1:c.1693G>T
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XP_011525056.1:p.Glu565Ter
|
|
NM_000175.5:c.1576G>T
MANE Select
|
NP_000166.2:p.Glu526Ter
|
|
NM_001289790.2:c.1492G>T
|
NP_001276719.1:p.Glu498Ter
|
|
NM_001329909.1:c.1576G>T
|
NP_001316838.1:p.Glu526Ter
|
|
NM_001329910.1:c.1576G>T
|
NP_001316839.1:p.Glu526Ter
|
|
NM_001329911.1:c.1549G>T
|
NP_001316840.1:p.Glu517Ter
|
|
XM_011526754.3:c.1693G>T
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XP_011525056.1:p.Glu565Ter
|
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NM_001289790.3:c.1492G>T
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NP_001276719.1:p.Glu498Ter
|
|
NM_001329911.2:c.1549G>T
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NP_001316840.1:p.Glu517Ter
|
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