ENST00000527168.6:n.810G>T
|
|
|
ENST00000529110.2:c.795G>T
|
ENSP00000435349.2:p.Leu265Phe
|
|
ENST00000529957.6:n.769G>T
|
|
|
ENST00000683366.1:c.*443G>T
|
ENSP00000507283.1:n.*443G>T
|
|
ENST00000683887.1:c.759G>T
|
ENSP00000506886.1:p.Leu253Phe
|
|
ENST00000684100.1:n.705G>T
|
|
|
ENST00000684126.1:n.845G>T
|
|
|
ENST00000684688.1:n.1336G>T
|
|
|
ENST00000204679.9:c.711G>T
MANE Select
|
ENSP00000204679.4:p.Leu237Phe
|
|
ENST00000204679.8:c.711G>T
|
ENSP00000204679.4:p.Leu237Phe
|
|
ENST00000527076.1:n.1934G>T
|
|
|
ENST00000527168.5:n.878G>T
|
|
|
ENST00000529957.5:n.810G>T
|
|
|
NM_032520.4:c.711G>T
|
NP_115909.1:p.Leu237Phe
|
|
XM_017023782.1:c.759G>T
|
XP_016879271.1:p.Leu253Phe
|
|
XM_017023783.1:c.351G>T
|
XP_016879272.1:p.Leu117Phe
|
|
NM_032520.5:c.711G>T
MANE Select
|
NP_115909.1:p.Leu237Phe
|
|