ENST00000216714.8:c.674G>T
MANE Select
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ENSP00000216714.3:p.Gly225Val
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ENST00000216714.7:c.674G>T
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ENSP00000216714.3:p.Gly225Val
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ENST00000398030.8:c.674G>T
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ENSP00000381111.4:p.Gly225Val
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ENST00000553555.5:n.1094G>T
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ENST00000553681.5:c.674G>T
|
ENSP00000451327.1:p.Gly225Val
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ENST00000555414.5:c.674G>T
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ENSP00000451979.1:p.Gly225Val
|
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ENST00000555839.5:c.587G>T
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ENSP00000452460.1:p.Gly196Val
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ENST00000557054.1:c.*85G>T
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ENSP00000452212.2:n.*85G>T
|
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ENST00000557159.5:n.1290G>T
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ENST00000557365.1:n.754G>T
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NM_001244249.1:c.674G>T
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NP_001231178.1:p.Gly225Val
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NM_001641.3:c.674G>T
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NP_001632.2:p.Gly225Val
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NM_080648.2:c.674G>T
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NP_542379.1:p.Gly225Val
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NM_080649.2:c.674G>T
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NP_542380.1:p.Gly225Val
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XM_005267581.3:c.674G>T
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XP_005267638.1:p.Gly225Val
|
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XM_005267582.3:c.623G>T
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XP_005267639.1:p.Gly208Val
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NM_001641.4:c.674G>T
MANE Select
|
NP_001632.2:p.Gly225Val
|
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NM_001244249.2:c.674G>T
|
NP_001231178.1:p.Gly225Val
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NM_080648.3:c.674G>T
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NP_542379.1:p.Gly225Val
|
|
NM_080649.3:c.674G>T
|
NP_542380.1:p.Gly225Val
|
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