ENST00000224721.12:c.7365T>C
MANE Select
|
ENSP00000224721.9:p.Gly2455=
|
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ENST00000642965.1:c.1298T>C
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ENSP00000495222.1:n.1298T>C
|
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ENST00000647092.1:c.962T>C
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ENSP00000495176.1:n.962T>C
|
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ENST00000224721.10:c.7380T>C
|
ENSP00000224721.8:p.Gly2460=
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|
ENST00000398788.4:c.645T>C
|
ENSP00000381768.3:p.Gly215=
|
|
ENST00000475158.1:n.901T>C
|
|
|
ENST00000619887.4:c.645T>C
|
ENSP00000478374.1:p.Gly215=
|
|
ENST00000622827.4:c.7365T>C
|
ENSP00000483211.1:p.Gly2455=
|
|
NM_001171933.1:c.645T>C
|
NP_001165404.1:p.Gly215=
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|
NM_001171934.1:c.645T>C
|
NP_001165405.1:p.Gly215=
|
|
NM_022124.5:c.7365T>C
|
NP_071407.4:p.Gly2455=
|
|
XM_006717940.2:c.7560T>C
|
XP_006718003.1:p.Gly2520=
|
|
XM_006717942.2:c.7494T>C
|
XP_006718005.1:p.Gly2498=
|
|
XM_011540039.1:c.7557T>C
|
XP_011538341.1:p.Gly2519=
|
|
XM_011540040.1:c.7554T>C
|
XP_011538342.1:p.Gly2518=
|
|
XM_011540041.1:c.7500T>C
|
XP_011538343.1:p.Gly2500=
|
|
XM_011540042.1:c.7470T>C
|
XP_011538344.1:p.Gly2490=
|
|
XM_011540043.1:c.7560T>C
|
XP_011538345.1:p.Gly2520=
|
|
XM_011540044.1:c.7425T>C
|
XP_011538346.1:p.Gly2475=
|
|
XM_011540045.1:c.7560T>C
|
XP_011538347.1:p.Gly2520=
|
|
XM_011540046.1:c.7020T>C
|
XP_011538348.1:p.Gly2340=
|
|
XM_011540047.1:c.6378T>C
|
XP_011538349.1:p.Gly2126=
|
|
XM_011540052.1:c.3888T>C
|
XP_011538354.1:p.Gly1296=
|
|
NM_022124.6:c.7365T>C
MANE Select
|
NP_071407.4:p.Gly2455=
|
|