ENST00000527168.6:n.621G>C
|
|
|
ENST00000529110.2:c.606G>C
|
ENSP00000435349.2:p.Leu202Phe
|
|
ENST00000529957.6:n.580G>C
|
|
|
ENST00000683366.1:c.*254G>C
|
ENSP00000507283.1:n.*254G>C
|
|
ENST00000683887.1:c.570G>C
|
ENSP00000506886.1:p.Leu190Phe
|
|
ENST00000684100.1:n.516G>C
|
|
|
ENST00000684126.1:n.580G>C
|
|
|
ENST00000684688.1:n.1147G>C
|
|
|
ENST00000204679.9:c.522G>C
MANE Select
|
ENSP00000204679.4:p.Leu174Phe
|
|
ENST00000204679.8:c.522G>C
|
ENSP00000204679.4:p.Leu174Phe
|
|
ENST00000527076.1:n.1538G>C
|
|
|
ENST00000527168.5:n.558G>C
|
|
|
ENST00000529957.5:n.621G>C
|
|
|
NM_032520.4:c.522G>C
|
NP_115909.1:p.Leu174Phe
|
|
XM_017023782.1:c.570G>C
|
XP_016879271.1:p.Leu190Phe
|
|
XM_017023783.1:c.162G>C
|
XP_016879272.1:p.Leu54Phe
|
|
NM_032520.5:c.522G>C
MANE Select
|
NP_115909.1:p.Leu174Phe
|
|