ENST00000532405.6:c.1255+11276C>T
MANE Select
|
ENSP00000431840.1:n.1255+11276C>T
|
|
ENST00000676001.1:c.1255+11276C>T
|
ENSP00000502715.1:n.1255+11276C>T
|
|
ENST00000393265.6:c.1063+11276C>T
|
ENSP00000376948.2:n.1063+11276C>T
|
|
ENST00000525557.5:c.851+11276C>T
|
|
|
ENST00000526482.1:n.1509+11276C>T
|
|
|
ENST00000531433.5:c.1198+11276C>T
|
ENSP00000433302.1:n.1198+11276C>T
|
|
ENST00000532405.5:c.1255+11276C>T
|
ENSP00000431840.1:n.1255+11276C>T
|
|
ENST00000554925.5:n.708+11276C>T
|
|
|
NM_153646.3:c.1255+11276C>T
|
NP_705932.2:n.1255+11276C>T
|
|
NM_153647.3:c.1198+11276C>T
|
NP_705933.2:n.1198+11276C>T
|
|
NM_153648.3:c.1063+11276C>T
|
NP_705934.1:n.1063+11276C>T
|
|
XM_005267342.1:c.811+11276C>T
|
XP_005267399.1:n.811+11276C>T
|
|
XM_011536436.1:c.1396+11276C>T
|
XP_011534738.1:n.1396+11276C>T
|
|
XM_011536437.1:c.1339+11276C>T
|
XP_011534739.1:n.1339+11276C>T
|
|
XM_011536438.1:c.1396+11276C>T
|
XP_011534740.1:n.1396+11276C>T
|
|
XM_011536439.1:c.1339+11276C>T
|
XP_011534741.1:n.1339+11276C>T
|
|
XM_011536440.1:c.505+11276C>T
|
XP_011534742.1:n.505+11276C>T
|
|
XM_011536441.1:c.337+11276C>T
|
XP_011534743.1:n.337+11276C>T
|
|
XM_011536442.1:c.337+11276C>T
|
XP_011534744.1:n.337+11276C>T
|
|
XM_005267342.2:c.811+11276C>T
|
XP_005267399.1:n.811+11276C>T
|
|
XM_011536436.2:c.1396+11276C>T
|
XP_011534738.1:n.1396+11276C>T
|
|
XM_011536437.2:c.1339+11276C>T
|
XP_011534739.1:n.1339+11276C>T
|
|
XM_011536438.2:c.1396+11276C>T
|
XP_011534740.1:n.1396+11276C>T
|
|
XM_011536439.2:c.1339+11276C>T
|
XP_011534741.1:n.1339+11276C>T
|
|
XM_011536440.2:c.505+11276C>T
|
XP_011534742.1:n.505+11276C>T
|
|
XM_024449478.1:c.1198+11276C>T
|
XP_024305246.1:n.1198+11276C>T
|
|
NM_153647.4:c.1198+11276C>T
|
NP_705933.2:n.1198+11276C>T
|
|
NM_001378620.1:c.1255+11276C>T
|
NP_001365549.1:n.1255+11276C>T
|
|
NM_153646.4:c.1255+11276C>T
MANE Select
|
NP_705932.2:n.1255+11276C>T
|
|
NM_153648.4:c.1063+11276C>T
|
NP_705934.1:n.1063+11276C>T
|
|