ENST00000402696.9:c.1840G>T
MANE Select
|
ENSP00000385834.3:p.Ala614Ser
|
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ENST00000402696.7:c.1840G>T
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ENSP00000385834.3:p.Ala614Ser
|
|
ENST00000461695.1:c.571G>T
|
|
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ENST00000467842.1:n.2834G>T
|
|
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NM_001063.3:c.1840G>T
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NP_001054.1:p.Ala614Ser
|
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XM_011513100.1:c.1840G>T
|
XP_011511402.1:p.Ala614Ser
|
|
NM_001354703.1:c.1708G>T
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NP_001341632.1:p.Ala570Ser
|
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NM_001354704.1:c.1459G>T
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NP_001341633.1:p.Ala487Ser
|
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NM_001063.4:c.1840G>T
MANE Select
|
NP_001054.2:p.Ala614Ser
|
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NM_001354703.2:c.1708G>T
|
NP_001341632.2:p.Ala570Ser
|
|
NM_001354704.2:c.1459G>T
|
NP_001341633.2:p.Ala487Ser
|
|