ENST00000388996.10:c.997G>T
MANE Select
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ENSP00000373648.3:p.Ala333Ser
|
|
ENST00000521134.6:c.637G>T
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ENSP00000429799.1:p.Ala213Ser
|
|
ENST00000638588.1:c.670G>T
|
ENSP00000491940.1:p.Ala224Ser
|
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ENST00000639358.1:c.647G>T
|
|
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ENST00000639496.1:c.670G>T
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ENSP00000491165.1:p.Ala224Ser
|
|
ENST00000388996.8:c.997G>T
|
ENSP00000373648.3:p.Ala333Ser
|
|
ENST00000519445.5:c.997G>T
|
ENSP00000428790.1:p.Ala333Ser
|
|
ENST00000519589.1:n.775G>T
|
|
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ENST00000521134.5:c.637G>T
|
ENSP00000429799.1:p.Ala213Ser
|
|
ENST00000621976.1:c.634G>T
|
ENSP00000482510.1:p.Ala212Ser
|
|
NM_001204824.1:c.637G>T
|
NP_001191753.1:p.Ala213Ser
|
|
NM_004519.3:c.997G>T
|
NP_004510.1:p.Ala333Ser
|
|
XM_005250914.2:c.-160G>T
|
XP_005250971.1:n.-160G>T
|
|
XM_006716555.2:c.289G>T
|
XP_006716618.1:p.Ala97Ser
|
|
XM_011517026.1:c.637G>T
|
XP_011515328.1:p.Ala213Ser
|
|
XM_005250914.3:c.-160G>T
|
XP_005250971.1:n.-160G>T
|
|
XM_006716555.3:c.289G>T
|
XP_006716618.1:p.Ala97Ser
|
|
XM_011517026.2:c.637G>T
|
XP_011515328.1:p.Ala213Ser
|
|
XM_017013400.1:c.775G>T
|
XP_016868889.1:p.Ala259Ser
|
|
NM_004519.4:c.997G>T
MANE Select
|
NP_004510.1:p.Ala333Ser
|
|
NM_001204824.2:c.637G>T
|
NP_001191753.1:p.Ala213Ser
|
|