ENST00000506729.6:c.1856G>C
MANE Select
|
ENSP00000421339.1:p.Ser619Thr
|
|
ENST00000379807.7:c.1856G>C
|
ENSP00000369135.3:p.Ser619Thr
|
|
ENST00000389019.7:c.1670G>C
|
ENSP00000373671.3:p.Ser557Thr
|
|
ENST00000506729.5:c.1856G>C
|
ENSP00000421339.1:p.Ser619Thr
|
|
ENST00000513675.1:c.1097G>C
|
ENSP00000421990.1:p.Ser366Thr
|
|
ENST00000514765.6:n.226G>C
|
|
|
NM_001289002.1:c.1856G>C
|
NP_001275931.1:p.Ser619Thr
|
|
NM_001289004.1:c.1670G>C
|
NP_001275933.1:p.Ser557Thr
|
|
NM_001308014.1:c.1097G>C
|
NP_001294943.1:p.Ser366Thr
|
|
NM_173488.4:c.1856G>C
|
NP_775759.3:p.Ser619Thr
|
|
XM_005271874.2:c.1856G>C
|
XP_005271931.1:p.Ser619Thr
|
|
XM_011543147.1:c.1751G>C
|
XP_011541449.1:p.Ser584Thr
|
|
XM_011543148.1:c.1619G>C
|
XP_011541450.1:p.Ser540Thr
|
|
XM_011543149.1:c.1283G>C
|
XP_011541451.1:p.Ser428Thr
|
|
XM_011543150.1:c.1127G>C
|
XP_011541452.1:p.Ser376Thr
|
|
XM_011543151.1:c.1097G>C
|
XP_011541453.1:p.Ser366Thr
|
|
XM_011543153.1:c.1034G>C
|
XP_011541455.1:p.Ser345Thr
|
|
XM_005271874.3:c.1856G>C
|
XP_005271931.1:p.Ser619Thr
|
|
XM_011543147.2:c.1751G>C
|
XP_011541449.1:p.Ser584Thr
|
|
XM_011543148.2:c.1619G>C
|
XP_011541450.1:p.Ser540Thr
|
|
XM_011543153.2:c.1034G>C
|
XP_011541455.1:p.Ser345Thr
|
|
NM_001289002.2:c.1856G>C
|
NP_001275931.1:p.Ser619Thr
|
|
NM_001289004.2:c.1670G>C
|
NP_001275933.1:p.Ser557Thr
|
|
NM_001308014.2:c.1097G>C
|
NP_001294943.1:p.Ser366Thr
|
|
NM_173488.5:c.1856G>C
MANE Select
|
NP_775759.3:p.Ser619Thr
|
|