ENST00000407991.3:c.1290C>T
MANE Select
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ENSP00000385026.1:p.Ala430=
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ENST00000240132.7:c.1245C>T
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ENSP00000240132.2:p.Ala415=
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ENST00000407991.2:c.1290C>T
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ENSP00000385026.1:p.Ala430=
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ENST00000520600.1:n.290-1399C>T
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|
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ENST00000520933.7:c.1224C>T
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ENSP00000429616.2:p.Ala408=
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ENST00000523695.5:c.*692C>T
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ENSP00000430612.1:n.*692C>T
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NM_000742.3:c.1290C>T
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NP_000733.2:p.Ala430=
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NM_001282455.1:c.1245C>T
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NP_001269384.1:p.Ala415=
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XM_005273397.1:c.813C>T
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XP_005273454.1:p.Ala271=
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XM_006716282.1:c.1290C>T
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XP_006716345.1:p.Ala430=
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XM_011544388.1:c.1290C>T
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XP_011542690.1:p.Ala430=
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XM_011544389.1:c.696C>T
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XP_011542691.1:p.Ala232=
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NM_001347705.1:c.813C>T
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NP_001334634.1:p.Ala271=
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NM_001347706.1:c.813C>T
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NP_001334635.1:p.Ala271=
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NM_001347707.1:c.696C>T
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NP_001334636.1:p.Ala232=
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NM_001347708.1:c.696C>T
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NP_001334637.1:p.Ala232=
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XM_011544389.2:c.696C>T
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XP_011542691.1:p.Ala232=
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NM_000742.4:c.1290C>T
MANE Select
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NP_000733.2:p.Ala430=
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NM_001282455.2:c.1245C>T
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NP_001269384.1:p.Ala415=
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|
NM_001347705.2:c.813C>T
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NP_001334634.1:p.Ala271=
|
|
NM_001347706.2:c.813C>T
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NP_001334635.1:p.Ala271=
|
|
NM_001347707.2:c.696C>T
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NP_001334636.1:p.Ala232=
|
|
NM_001347708.2:c.696C>T
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NP_001334637.1:p.Ala232=
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