ENST00000394867.9:n.1356G>C
|
|
|
ENST00000687128.1:n.1356G>C
|
|
|
ENST00000688002.1:n.1211G>C
|
|
|
ENST00000689792.1:n.821G>C
|
|
|
ENST00000262948.10:c.917G>C
MANE Select
|
ENSP00000262948.4:p.Ser306Thr
|
|
ENST00000262948.9:c.917G>C
|
ENSP00000262948.3:p.Ser306Thr
|
|
ENST00000394867.8:c.626G>C
|
ENSP00000378336.1:p.Ser209Thr
|
|
ENST00000593364.5:n.864G>C
|
|
|
ENST00000595715.1:n.732G>C
|
|
|
ENST00000597263.5:n.169+1816G>C
|
|
|
ENST00000599021.1:c.29+1816G>C
|
|
|
ENST00000600584.5:n.1477G>C
|
|
|
ENST00000601786.5:n.1218G>C
|
|
|
NM_030662.3:c.917G>C , LRG_750t1:c.917G>C
|
NP_109587.1:p.Ser306Thr
|
|
XM_006722799.2:c.705+1816G>C
|
XP_006722862.1:n.705+1816G>C
|
|
XM_011528133.1:c.347G>C
|
XP_011526435.1:p.Ser116Thr
|
|
XM_017026989.1:c.917G>C
|
XP_016882478.1:p.Ser306Thr
|
|
XM_017026990.1:c.705+1816G>C
|
XP_016882479.1:n.705+1816G>C
|
|
NM_030662.4:c.917G>C
MANE Select
|
NP_109587.1:p.Ser306Thr
|
|