|
NM_145290.4:c.1659G>C
MANE Select
|
NP_660333.2:p.Thr553=
|
|
ENST00000334304.10:c.1659G>C
MANE Select
|
ENSP00000334952.5:p.Thr553=
|
|
NM_145290.3:c.1659G>C
|
NP_660333.2:p.Thr553=
|
|
ENST00000282943.9:n.1284G>C
|
|
|
ENST00000334304.9:c.1659G>C
|
ENSP00000334952.5:p.Thr553=
|
|
ENST00000502482.1:c.1659G>C
|
ENSP00000421006.1:p.Thr553=
|
|
ENST00000508133.5:c.981G>C
|
ENSP00000422606.1:p.Thr327=
|
|
XM_005248137.3:c.1659G>C
|
XP_005248194.1:p.Thr553=
|
|
XM_005248137.5:c.1659G>C
|
XP_005248194.1:p.Thr553=
|
|
XM_011513810.1:c.1068G>C
|
XP_011512112.1:p.Thr356=
|
|
XM_011513811.1:c.981G>C
|
XP_011512113.1:p.Thr327=
|
|
XM_011513811.2:c.981G>C
|
XP_011512113.1:p.Thr327=
|
|
XR_001741153.1:n.1933G>C
|
|
|
XR_925316.1:n.1933G>C
|
|