ENST00000303941.4:c.1295T=
MANE Select
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ENSP00000306678.3:p.Leu432=
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ENST00000303941.3:c.1295T=
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ENSP00000306678.3:p.Leu432=
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NM_178510.1:c.1295T=
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NP_848605.1:p.Leu432=
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XM_011542736.1:c.1328T=
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XP_011541038.1:p.Leu443=
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XM_011542737.1:c.1298T=
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XP_011541039.1:p.Leu433=
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XM_011542738.1:c.1106T=
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XP_011541040.1:p.Leu369=
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XM_011542736.2:c.1328T=
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XP_011541038.1:p.Leu443=
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XM_011542737.2:c.1298T=
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XP_011541039.1:p.Leu433=
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XM_011542738.2:c.1106T=
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XP_011541040.1:p.Leu369=
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XM_017017475.1:c.1325T=
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XP_016872964.1:p.Leu442=
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NM_178510.2:c.1295T=
MANE Select
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NP_848605.1:p.Leu432=
|
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