ENST00000523022.6:c.764G>C
MANE Select
|
ENSP00000429798.1:p.Arg255Thr
|
|
ENST00000431316.3:c.764G>C
|
ENSP00000392338.1:p.Arg255Thr
|
|
ENST00000521679.5:c.513G>C
|
|
|
ENST00000522389.5:c.362G>C
|
ENSP00000427773.1:p.Arg121Thr
|
|
ENST00000523022.5:c.764G>C
|
ENSP00000429798.1:p.Arg255Thr
|
|
ENST00000523953.5:c.764G>C
|
ENSP00000430656.1:p.Arg255Thr
|
|
ENST00000524324.5:c.566G>C
|
ENSP00000428923.1:p.Arg189Thr
|
|
ENST00000542576.5:c.764G>C
|
ENSP00000443517.1:p.Arg255Thr
|
|
ENST00000626824.1:c.362G>C
|
ENSP00000486171.1:p.Arg121Thr
|
|
NM_001128829.3:c.764G>C
|
NP_001122301.1:p.Arg255Thr
|
|
NM_001128830.3:c.764G>C
|
NP_001122302.1:p.Arg255Thr
|
|
NM_001128831.3:c.764G>C
|
NP_001122303.1:p.Arg255Thr
|
|
NM_001164830.1:c.764G>C
|
NP_001158302.1:p.Arg255Thr
|
|
NM_001291967.1:c.566G>C
|
NP_001278896.1:p.Arg189Thr
|
|
NM_001291968.1:c.425G>C
|
NP_001278897.1:p.Arg142Thr
|
|
NM_001738.4:c.764G>C
|
NP_001729.1:p.Arg255Thr
|
|
XM_011517584.1:c.764G>C
|
XP_011515886.1:p.Arg255Thr
|
|
NM_001128829.4:c.764G>C
|
NP_001122301.1:p.Arg255Thr
|
|
NM_001128830.4:c.764G>C
|
NP_001122302.1:p.Arg255Thr
|
|
NM_001128831.4:c.764G>C
MANE Select
|
NP_001122303.1:p.Arg255Thr
|
|
NM_001164830.2:c.764G>C
|
NP_001158302.1:p.Arg255Thr
|
|
NM_001291967.2:c.566G>C
|
NP_001278896.1:p.Arg189Thr
|
|
NM_001291968.2:c.425G>C
|
NP_001278897.1:p.Arg142Thr
|
|
NM_001738.5:c.764G>C
|
NP_001729.1:p.Arg255Thr
|
|