ENST00000388996.10:c.926G>C
MANE Select
|
ENSP00000373648.3:p.Trp309Ser
|
|
ENST00000521134.6:c.566G>C
|
ENSP00000429799.1:p.Trp189Ser
|
|
ENST00000638588.1:c.599G>C
|
ENSP00000491940.1:p.Trp200Ser
|
|
ENST00000639358.1:c.576G>C
|
|
|
ENST00000639496.1:c.599G>C
|
ENSP00000491165.1:p.Trp200Ser
|
|
ENST00000388996.8:c.926G>C
|
ENSP00000373648.3:p.Trp309Ser
|
|
ENST00000519445.5:c.926G>C
|
ENSP00000428790.1:p.Trp309Ser
|
|
ENST00000519589.1:n.704G>C
|
|
|
ENST00000521134.5:c.566G>C
|
ENSP00000429799.1:p.Trp189Ser
|
|
ENST00000621976.1:c.563G>C
|
ENSP00000482510.1:p.Trp188Ser
|
|
NM_001204824.1:c.566G>C
|
NP_001191753.1:p.Trp189Ser
|
|
NM_004519.3:c.926G>C
|
NP_004510.1:p.Trp309Ser
|
|
XM_005250914.2:c.-231G>C
|
XP_005250971.1:n.-231G>C
|
|
XM_006716555.2:c.218G>C
|
XP_006716618.1:p.Trp73Ser
|
|
XM_011517026.1:c.566G>C
|
XP_011515328.1:p.Trp189Ser
|
|
XM_005250914.3:c.-231G>C
|
XP_005250971.1:n.-231G>C
|
|
XM_006716555.3:c.218G>C
|
XP_006716618.1:p.Trp73Ser
|
|
XM_011517026.2:c.566G>C
|
XP_011515328.1:p.Trp189Ser
|
|
XM_017013400.1:c.704G>C
|
XP_016868889.1:p.Trp235Ser
|
|
NM_004519.4:c.926G>C
MANE Select
|
NP_004510.1:p.Trp309Ser
|
|
NM_001204824.2:c.566G>C
|
NP_001191753.1:p.Trp189Ser
|
|