ENST00000376883.2:c.1349G>T
MANE Select
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ENSP00000366080.2:p.Gly450Val
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ENST00000488757.6:c.1133G>T
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ENSP00000418259.2:p.Gly378Val
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|
ENST00000376881.4:c.1097G>T
|
ENSP00000366078.4:p.Gly366Val
|
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ENST00000376883.1:c.1289G>T
|
ENSP00000366080.1:p.Gly430Val
|
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ENST00000488757.5:c.1349G>T
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ENSP00000418259.1:p.Gly450Val
|
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NM_001109809.2:c.1349G>T
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NP_001103279.2:p.Gly450Val
|
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XM_006715087.2:c.1133G>T
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XP_006715150.1:p.Gly378Val
|
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XM_011514570.1:c.1349G>T
|
XP_011512872.1:p.Gly450Val
|
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NM_001109809.3:c.1349G>T
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NP_001103279.2:p.Gly450Val
|
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NM_001366333.1:c.1133G>T
|
NP_001353262.1:p.Gly378Val
|
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NM_001109809.4:c.1349G>T
|
NP_001103279.2:p.Gly450Val
|
|
NM_001366333.2:c.1133G>T
|
NP_001353262.1:p.Gly378Val
|
|
NM_001109809.5:c.1349G>T
MANE Select
|
NP_001103279.2:p.Gly450Val
|
|