ENST00000308736.7:c.1270G>A
MANE Select
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ENSP00000311135.2:p.Ala424Thr
|
|
ENST00000544745.2:c.741G>A
|
|
|
ENST00000679875.1:n.1342G>A
|
|
|
ENST00000308736.6:c.1270G>A
|
ENSP00000311135.2:p.Ala424Thr
|
|
ENST00000539298.1:n.1370G>A
|
|
|
ENST00000544745.1:c.631G>A
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ENSP00000439009.1:p.Ala211Thr
|
|
NM_032656.3:c.1270G>A
|
NP_116045.2:p.Ala424Thr
|
|
XM_005253590.2:c.1270G>A
|
XP_005253647.1:p.Ala424Thr
|
|
XM_011538597.1:c.1270G>A
|
XP_011536899.1:p.Ala424Thr
|
|
XM_011538598.1:c.1270G>A
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XP_011536900.1:p.Ala424Thr
|
|
XM_011538599.1:c.1270G>A
|
XP_011536901.1:p.Ala424Thr
|
|
XM_011538600.1:c.1270G>A
|
XP_011536902.1:p.Ala424Thr
|
|
XM_005253590.3:c.1270G>A
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XP_005253647.1:p.Ala424Thr
|
|
XM_011538598.2:c.1270G>A
|
XP_011536900.1:p.Ala424Thr
|
|
XM_011538600.2:c.1270G>A
|
XP_011536902.1:p.Ala424Thr
|
|
XR_001748819.1:n.1373G>A
|
|
|
XR_001748820.1:n.1373G>A
|
|
|
NM_032656.4:c.1270G>A
MANE Select
|
NP_116045.2:p.Ala424Thr
|
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