ENST00000261609.13:c.11816+12A>C
MANE Select
|
ENSP00000261609.8:n.11816+12A>C
|
|
ENST00000650509.1:c.3527+12A>C
|
ENSP00000496936.1:n.3527+12A>C
|
|
ENST00000261609.11:c.11816+12A>C
|
ENSP00000261609.7:n.11816+12A>C
|
|
NM_004667.5:c.11816+12A>C
|
NP_004658.3:n.11816+12A>C
|
|
XM_005268276.3:c.11702+12A>C
|
XP_005268333.1:n.11702+12A>C
|
|
XM_005268277.3:c.11702+12A>C
|
XP_005268334.1:n.11702+12A>C
|
|
XM_006720726.2:c.11801+12A>C
|
XP_006720789.1:n.11801+12A>C
|
|
XM_006720727.2:c.11558+12A>C
|
XP_006720790.1:n.11558+12A>C
|
|
XM_011522131.1:c.11333+12A>C
|
XP_011520433.1:n.11333+12A>C
|
|
XM_011522132.1:c.9332+12A>C
|
XP_011520434.1:n.9332+12A>C
|
|
XM_011522133.1:c.8561+12A>C
|
XP_011520435.1:n.8561+12A>C
|
|
XM_011522134.1:c.5933+12A>C
|
XP_011520436.1:n.5933+12A>C
|
|
XM_005268276.5:c.11702+12A>C
|
XP_005268333.1:n.11702+12A>C
|
|
XM_006720726.3:c.11801+12A>C
|
XP_006720789.1:n.11801+12A>C
|
|
XM_006720727.3:c.11558+12A>C
|
XP_006720790.1:n.11558+12A>C
|
|
XM_017022695.1:c.11702+12A>C
|
XP_016878184.1:n.11702+12A>C
|
|
XM_017022696.1:c.11702+12A>C
|
XP_016878185.1:n.11702+12A>C
|
|
XM_017022697.1:c.4982+12A>C
|
XP_016878186.1:n.4982+12A>C
|
|
XM_017022698.1:c.4982+12A>C
|
XP_016878187.1:n.4982+12A>C
|
|
NM_004667.6:c.11816+12A>C
MANE Select
|
NP_004658.3:n.11816+12A>C
|
|