ENST00000264499.9:c.602G>T
MANE Select
|
ENSP00000264499.4:p.Gly201Val
|
|
ENST00000264499.8:c.602G>T
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ENSP00000264499.4:p.Gly201Val
|
|
ENST00000506636.1:c.602G>T
|
ENSP00000423626.1:p.Gly201Val
|
|
NM_018190.3:c.602G>T
|
NP_060660.2:p.Gly201Val
|
|
NM_176824.2:c.602G>T
|
NP_789794.1:p.Gly201Val
|
|
XM_005263106.2:c.605G>T
|
XP_005263163.1:p.Gly202Val
|
|
XM_011532079.1:c.650G>T
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XP_011530381.1:p.Gly217Val
|
|
XM_011532080.1:c.647G>T
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XP_011530382.1:p.Ser216Ile
|
|
XM_011532081.1:c.650G>T
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XP_011530383.1:p.Gly217Val
|
|
XM_005263106.4:c.605G>T
|
XP_005263163.1:p.Gly202Val
|
|
XM_011532079.3:c.650G>T
|
XP_011530381.1:p.Gly217Val
|
|
XM_011532080.3:c.647G>T
|
XP_011530382.1:p.Ser216Ile
|
|
XM_011532081.3:c.650G>T
|
XP_011530383.1:p.Gly217Val
|
|
XM_017008357.2:c.602G>T
|
XP_016863846.1:p.Gly201Val
|
|
XM_017008358.2:c.605G>T
|
XP_016863847.1:p.Gly202Val
|
|
NM_176824.3:c.602G>T
MANE Select
|
NP_789794.1:p.Gly201Val
|
|
NM_018190.4:c.602G>T
|
NP_060660.2:p.Gly201Val
|
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