ENST00000470094.2:c.*416T>C
|
ENSP00000434898.2:n.*416T>C
|
|
ENST00000528762.2:c.*1260T>C
|
ENSP00000433168.2:n.*1260T>C
|
|
ENST00000530893.7:c.9524T>C
|
ENSP00000499438.2:p.Phe3175Ser
|
|
ENST00000665585.2:c.*1455T>C
|
ENSP00000499570.2:n.*1455T>C
|
|
ENST00000700202.2:c.9842T>C
|
ENSP00000514856.2:p.Phe3281Ser
|
|
ENST00000700202.1:c.2309T>C
|
ENSP00000514856.1:p.Phe770Ser
|
|
ENST00000700203.1:n.2020T>C
|
|
|
ENST00000380152.8:c.9893T>C
MANE Select
|
ENSP00000369497.3:p.Phe3298Ser
|
|
ENST00000544455.6:c.9893T>C
|
ENSP00000439902.1:p.Phe3298Ser
|
|
ENST00000614259.2:c.9901T>C
|
ENSP00000506251.1:n.9901T>C
|
|
ENST00000680887.1:c.9893T>C
|
ENSP00000505508.1:p.Phe3298Ser
|
|
ENST00000380152.7:c.9893T>C
|
ENSP00000369497.3:p.Phe3298Ser
|
|
ENST00000533776.1:n.481T>C
|
|
|
ENST00000544455.5:c.9893T>C
|
ENSP00000439902.1:p.Phe3298Ser
|
|
NM_000059.3:c.9893T>C , LRG_293t1:c.9893T>C
|
NP_000050.2:p.Phe3298Ser
|
|
XM_011535203.1:c.9893T>C
|
XP_011533505.1:p.Phe3298Ser
|
|
XM_011535204.1:c.9797T>C
|
XP_011533506.1:p.Phe3266Ser
|
|
NM_000059.4:c.9893T>C
MANE Select
|
NP_000050.3:p.Phe3298Ser
|
|