ENST00000317961.9:c.4560T>C
MANE Select
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ENSP00000322408.4:p.Ala1520=
|
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ENST00000317961.8:c.4560T>C
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ENSP00000322408.4:p.Ala1520=
|
|
ENST00000382806.6:c.4389T>C
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ENSP00000372256.2:p.Ala1463=
|
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ENST00000469599.6:n.3311T>C
|
|
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ENST00000492117.1:n.4605T>C
|
|
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ENST00000541639.5:c.4653T>C
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ENSP00000444293.1:p.Ala1551=
|
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NM_001146705.1:c.4653T>C
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NP_001140177.1:p.Ala1551=
|
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NM_001146706.1:c.4389T>C
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NP_001140178.1:p.Ala1463=
|
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NM_004653.4:c.4560T>C
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NP_004644.2:p.Ala1520=
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XM_005262560.1:c.4425T>C
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XP_005262617.1:p.Ala1475=
|
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XM_005262561.1:c.4329T>C
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XP_005262618.1:p.Ala1443=
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XM_011531468.1:c.4482T>C
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XP_011529770.1:p.Ala1494=
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XR_430568.2:n.5335T>C
|
|
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XM_005262560.3:c.4425T>C
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XP_005262617.1:p.Ala1475=
|
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XM_005262561.3:c.4329T>C
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XP_005262618.1:p.Ala1443=
|
|
XM_011531468.3:c.4482T>C
|
XP_011529770.1:p.Ala1494=
|
|
XM_024452495.1:c.2550T>C
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XP_024308263.1:p.Ala850=
|
|
XM_024452496.1:c.2316T>C
|
XP_024308264.1:p.Ala772=
|
|
XR_001756009.2:n.5298T>C
|
|
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XR_001756010.2:n.5266T>C
|
|
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XR_001756011.2:n.5163T>C
|
|
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XR_001756012.2:n.5311T>C
|
|
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XR_001756013.2:n.4629T>C
|
|
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XR_002958832.1:n.4883T>C
|
|
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XR_002958834.1:n.4954T>C
|
|
|
XR_002958835.1:n.4837T>C
|
|
|
XR_002958836.1:n.5488T>C
|
|
|
XR_002958837.1:n.5295T>C
|
|
|
XR_244571.4:n.4815T>C
|
|
|
XR_430568.4:n.5334T>C
|
|
|
NM_001146706.2:c.4389T>C
|
NP_001140178.1:p.Ala1463=
|
|
NM_004653.5:c.4560T>C
MANE Select
|
NP_004644.2:p.Ala1520=
|
|
NM_001146705.2:c.4653T>C
|
NP_001140177.1:p.Ala1551=
|
|