ENST00000371568.8:c.2447T>C
MANE Select
|
ENSP00000360623.3:p.Met816Thr
|
|
ENST00000371566.1:c.2447T>C
|
ENSP00000360621.1:p.Met816Thr
|
|
ENST00000371568.7:c.2447T>C
|
ENSP00000360623.3:p.Met816Thr
|
|
NM_001190818.1:c.2447T>C
|
NP_001177747.1:p.Met816Thr
|
|
NM_001190819.1:c.2432T>C
|
NP_001177748.1:p.Met811Thr
|
|
NM_004153.3:c.2447T>C
|
NP_004144.2:p.Met816Thr
|
|
XM_011541527.1:c.1367T>C
|
XP_011539829.1:p.Met456Thr
|
|
XM_011541527.3:c.1367T>C
|
XP_011539829.1:p.Met456Thr
|
|
XM_017001388.2:c.2339T>C
|
XP_016856877.1:p.Met780Thr
|
|
XM_017001389.2:c.1709T>C
|
XP_016856878.1:p.Met570Thr
|
|
NM_004153.4:c.2447T>C
MANE Select
|
NP_004144.2:p.Met816Thr
|
|
NM_001190818.2:c.2447T>C
|
NP_001177747.1:p.Met816Thr
|
|
NM_001190819.2:c.2432T>C
|
NP_001177748.1:p.Met811Thr
|
|