ENST00000399503.4:c.804A=
MANE Select
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ENSP00000382423.3:p.Gly268=
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|
ENST00000399503.3:c.804A=
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ENSP00000382423.3:p.Gly268=
|
|
NM_005921.1:c.804A=
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NP_005912.1:p.Gly268=
|
|
XM_005248519.3:c.426A=
|
XP_005248576.2:p.Gly142=
|
|
XM_011543406.1:c.549A=
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XP_011541708.1:p.Gly183=
|
|
XM_011543407.1:c.804A=
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XP_011541709.1:p.Gly268=
|
|
XM_011543408.1:c.804A=
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XP_011541710.1:p.Gly268=
|
|
XM_017009484.1:c.393A=
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XP_016864973.1:p.Gly131=
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XM_017009485.1:c.315A=
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XP_016864974.1:p.Gly105=
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XR_001742068.2:n.835A=
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|
|
NM_005921.2:c.804A=
MANE Select
|
NP_005912.1:p.Gly268=
|
|