ENST00000527168.6:n.904C>T
|
|
|
ENST00000529110.2:c.889C>T
|
ENSP00000435349.2:p.Pro297Ser
|
|
ENST00000529957.6:n.863C>T
|
|
|
ENST00000683366.1:c.*537C>T
|
ENSP00000507283.1:n.*537C>T
|
|
ENST00000683887.1:c.853C>T
|
ENSP00000506886.1:p.Pro285Ser
|
|
ENST00000684100.1:n.799C>T
|
|
|
ENST00000684126.1:n.939C>T
|
|
|
ENST00000684688.1:n.1430C>T
|
|
|
ENST00000204679.9:c.805C>T
MANE Select
|
ENSP00000204679.4:p.Pro269Ser
|
|
ENST00000204679.8:c.805C>T
|
ENSP00000204679.4:p.Pro269Ser
|
|
ENST00000527076.1:n.2028C>T
|
|
|
ENST00000527168.5:n.972C>T
|
|
|
ENST00000529957.5:n.904C>T
|
|
|
NM_032520.4:c.805C>T
|
NP_115909.1:p.Pro269Ser
|
|
XM_017023782.1:c.853C>T
|
XP_016879271.1:p.Pro285Ser
|
|
XM_017023783.1:c.445C>T
|
XP_016879272.1:p.Pro149Ser
|
|
NM_032520.5:c.805C>T
MANE Select
|
NP_115909.1:p.Pro269Ser
|
|