ENST00000372470.9:c.1525G>T
MANE Select
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ENSP00000361548.3:p.Gly509Cys
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ENST00000413998.7:c.1504G>T
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ENSP00000414004.3:p.Gly502Cys
|
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ENST00000638732.1:n.1525G>T
|
|
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ENST00000643351.1:c.57G>T
|
|
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ENST00000372470.7:c.1525G>T
|
ENSP00000361548.3:p.Gly509Cys
|
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ENST00000413998.6:c.1525G>T
|
ENSP00000414004.2:p.Gly509Cys
|
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ENST00000612993.1:c.1525G>T
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ENSP00000480273.1:p.Gly509Cys
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NM_005373.2:c.1525G>T , LRG_510t1:c.1525G>T
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NP_005364.1:p.Gly509Cys
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XM_011541478.1:c.1504G>T
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XP_011539780.1:p.Gly502Cys
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XM_017001320.1:c.1696G>T
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XP_016856809.1:p.Gly566Cys
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NM_005373.3:c.1525G>T
MANE Select
|
NP_005364.1:p.Gly509Cys
|
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