ENST00000527168.6:n.439G>T
|
|
|
ENST00000529110.2:c.424G>T
|
ENSP00000435349.2:p.Ala142Ser
|
|
ENST00000529957.6:n.398G>T
|
|
|
ENST00000683366.1:c.*72G>T
|
ENSP00000507283.1:n.*72G>T
|
|
ENST00000683887.1:c.388G>T
|
ENSP00000506886.1:p.Ala130Ser
|
|
ENST00000684100.1:n.334G>T
|
|
|
ENST00000684126.1:n.398G>T
|
|
|
ENST00000684688.1:n.965G>T
|
|
|
ENST00000204679.9:c.340G>T
MANE Select
|
ENSP00000204679.4:p.Ala114Ser
|
|
ENST00000204679.8:c.340G>T
|
ENSP00000204679.4:p.Ala114Ser
|
|
ENST00000526820.5:c.*242G>T
|
ENSP00000434413.1:n.*242G>T
|
|
ENST00000527076.1:n.1356G>T
|
|
|
ENST00000527168.5:n.376G>T
|
|
|
ENST00000529110.1:c.407G>T
|
|
|
ENST00000529957.5:n.439G>T
|
|
|
NM_032520.4:c.340G>T
|
NP_115909.1:p.Ala114Ser
|
|
XM_017023782.1:c.388G>T
|
XP_016879271.1:p.Ala130Ser
|
|
XM_017023783.1:c.-21G>T
|
XP_016879272.1:n.-21G>T
|
|
NM_032520.5:c.340G>T
MANE Select
|
NP_115909.1:p.Ala114Ser
|
|