ENST00000504915.3:c.7119A>C
|
ENSP00000473355.2:p.Ser2373=
|
|
ENST00000505350.2:c.*7071A>C
|
ENSP00000481752.1:n.*7071A>C
|
|
ENST00000507379.6:c.7011A>C
|
ENSP00000423224.2:p.Ser2337=
|
|
ENST00000509732.6:c.7065A>C
|
ENSP00000426541.2:p.Ser2355=
|
|
ENST00000512211.7:c.7065A>C
|
ENSP00000423828.3:p.Ser2355=
|
|
ENST00000257430.9:c.7065A>C
MANE Select
|
ENSP00000257430.4:p.Ser2355=
|
|
ENST00000257430.8:c.7065A>C
|
ENSP00000257430.4:p.Ser2355=
|
|
ENST00000508376.6:c.7065A>C
|
ENSP00000427089.2:p.Ser2355=
|
|
ENST00000508624.5:c.*6387A>C
|
ENSP00000424265.1:n.*6387A>C
|
|
ENST00000520401.1:c.230+13687A>C
|
|
|
NM_000038.5:c.7065A>C
|
NP_000029.2:p.Ser2355=
|
|
NM_001127510.2:c.7065A>C
|
NP_001120982.1:p.Ser2355=
|
|
NM_001127511.2:c.7011A>C
|
NP_001120983.2:p.Ser2337=
|
|
NM_001354895.1:c.7065A>C
|
NP_001341824.1:p.Ser2355=
|
|
NM_001354896.1:c.7119A>C
|
NP_001341825.1:p.Ser2373=
|
|
NM_001354897.1:c.7095A>C
|
NP_001341826.1:p.Ser2365=
|
|
NM_001354898.1:c.6990A>C
|
NP_001341827.1:p.Ser2330=
|
|
NM_001354899.1:c.6981A>C
|
NP_001341828.1:p.Ser2327=
|
|
NM_001354900.1:c.6942A>C
|
NP_001341829.1:p.Ser2314=
|
|
NM_001354901.1:c.6888A>C
|
NP_001341830.1:p.Ser2296=
|
|
NM_001354902.1:c.6792A>C
|
NP_001341831.1:p.Ser2264=
|
|
NM_001354903.1:c.6762A>C
|
NP_001341832.1:p.Ser2254=
|
|
NM_001354904.1:c.6687A>C
|
NP_001341833.1:p.Ser2229=
|
|
NM_001354905.1:c.6585A>C
|
NP_001341834.1:p.Ser2195=
|
|
NM_001354906.1:c.6216A>C
|
NP_001341835.1:p.Ser2072=
|
|
NM_000038.6:c.7065A>C
MANE Select
|
NP_000029.2:p.Ser2355=
|
|
NM_001127510.3:c.7065A>C
|
NP_001120982.1:p.Ser2355=
|
|
NM_001127511.3:c.7011A>C
|
NP_001120983.2:p.Ser2337=
|
|
NM_001354895.2:c.7065A>C
|
NP_001341824.1:p.Ser2355=
|
|
NM_001354896.2:c.7119A>C
|
NP_001341825.1:p.Ser2373=
|
|
NM_001354897.2:c.7095A>C
|
NP_001341826.1:p.Ser2365=
|
|
NM_001354898.2:c.6990A>C
|
NP_001341827.1:p.Ser2330=
|
|
NM_001354899.2:c.6981A>C
|
NP_001341828.1:p.Ser2327=
|
|
NM_001354900.2:c.6942A>C
|
NP_001341829.1:p.Ser2314=
|
|
NM_001354901.2:c.6888A>C
|
NP_001341830.1:p.Ser2296=
|
|
NM_001354902.2:c.6792A>C
|
NP_001341831.1:p.Ser2264=
|
|
NM_001354903.2:c.6762A>C
|
NP_001341832.1:p.Ser2254=
|
|
NM_001354904.2:c.6687A>C
|
NP_001341833.1:p.Ser2229=
|
|
NM_001354905.2:c.6585A>C
|
NP_001341834.1:p.Ser2195=
|
|
NM_001354906.2:c.6216A>C
|
NP_001341835.1:p.Ser2072=
|
|