ENST00000242317.9:c.1879G>T
MANE Select
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ENSP00000242317.4:p.Ala627Ser
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ENST00000242317.8:c.1879G>T
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ENSP00000242317.4:p.Ala627Ser
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ENST00000442556.1:c.329+2606G>T
|
|
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ENST00000470169.5:c.667G>T
|
|
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ENST00000485580.1:n.455G>T
|
|
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ENST00000614641.4:c.1891G>T
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ENSP00000480538.1:p.Ala631Ser
|
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NM_001281428.1:c.1891G>T
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NP_001268357.1:p.Ala631Ser
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NM_012144.3:c.1879G>T
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NP_036276.1:p.Ala627Ser
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XM_006716758.2:c.1348G>T
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XP_006716821.1:p.Ala450Ser
|
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XM_011517848.1:c.1633G>T
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XP_011516150.1:p.Ala545Ser
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XM_006716758.3:c.1348G>T
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XP_006716821.1:p.Ala450Ser
|
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XM_011517848.2:c.1633G>T
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XP_011516150.1:p.Ala545Ser
|
|
XM_017014625.2:c.1621G>T
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XP_016870114.1:p.Ala541Ser
|
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XR_002956774.1:n.1982G>T
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|
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NM_012144.4:c.1879G>T
MANE Select
|
NP_036276.1:p.Ala627Ser
|
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NM_001281428.2:c.1891G>T
|
NP_001268357.1:p.Ala631Ser
|
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