ENST00000236671.7:c.955C>T
MANE Select
|
ENSP00000236671.2:p.Pro319Ser
|
|
ENST00000367196.4:c.850C>T
|
ENSP00000356164.4:p.Pro284Ser
|
|
ENST00000427721.3:c.380C>T
|
|
|
ENST00000429746.2:c.850C>T
|
ENSP00000402586.2:p.Pro284Ser
|
|
ENST00000433655.6:c.*121C>T
|
ENSP00000404902.1:n.*121C>T
|
|
ENST00000438213.6:c.1072C>T
|
ENSP00000415036.2:p.Pro358Ser
|
|
ENST00000497544.3:n.571C>T
|
|
|
ENST00000636397.1:c.955C>T
|
ENSP00000489910.1:p.Pro319Ser
|
|
ENST00000636571.1:c.934C>T
|
ENSP00000490770.1:p.Pro312Ser
|
|
ENST00000636615.1:c.955C>T
|
ENSP00000490014.1:p.Pro319Ser
|
|
ENST00000636843.1:c.949C>T
|
ENSP00000490897.1:p.Pro317Ser
|
|
ENST00000637158.1:n.553C>T
|
|
|
ENST00000637381.2:n.3383C>T
|
|
|
ENST00000637387.1:c.955C>T
|
ENSP00000490598.1:p.Pro319Ser
|
|
ENST00000637815.2:c.937C>T
|
ENSP00000490344.1:p.Pro313Ser
|
|
ENST00000637915.1:c.955C>T
|
ENSP00000490471.1:p.Pro319Ser
|
|
ENST00000637937.1:n.263C>T
|
|
|
ENST00000678991.1:c.*816C>T
|
ENSP00000503019.1:n.*816C>T
|
|
ENST00000236671.6:c.955C>T
|
ENSP00000236671.2:p.Pro319Ser
|
|
ENST00000427721.2:c.355C>T
|
ENSP00000415840.2:p.Pro119Ser
|
|
ENST00000429746.1:c.286C>T
|
ENSP00000402586.1:p.Pro96Ser
|
|
ENST00000433655.5:c.*121C>T
|
ENSP00000404902.1:n.*121C>T
|
|
ENST00000497544.1:n.571C>T
|
|
|
NM_001909.4:c.955C>T
|
NP_001900.1:p.Pro319Ser
|
|
NM_001909.5:c.955C>T
MANE Select
|
NP_001900.1:p.Pro319Ser
|
|