|
ENST00000265846.10:c.305+2793G>T
(ADAP1)
MANE Select
|
ENSP00000265846.5:n.305+2793G>T
|
|
|
ENST00000649206.1:c.305+2793G>T
(ADAP1)
|
ENSP00000497220.1:n.305+2793G>T
|
|
|
ENST00000265846.9:c.305+2793G>T
(ADAP1)
|
ENSP00000265846.5:n.305+2793G>T
|
|
|
ENST00000435943.1:c.266+2793G>T
(ADAP1)
|
ENSP00000394973.1:n.266+2793G>T
|
|
|
ENST00000446141.5:c.253+2793G>T
(ADAP1)
|
|
|
|
ENST00000449296.6:c.89+2793G>T
(ADAP1)
|
ENSP00000407267.2:n.89+2793G>T
|
|
|
ENST00000453823.5:c.133+2793G>T
(ADAP1)
|
|
|
|
ENST00000454383.5:c.126+2793G>T
(ADAP1)
|
|
|
|
ENST00000457254.5:c.*48+2793G>T
(COX19)
|
ENSP00000413423.1:n.*48+2793G>T
|
|
|
ENST00000463358.5:n.278+2793G>T
(ADAP1)
|
|
|
|
ENST00000477906.5:n.297+2793G>T
(ADAP1)
|
|
|
|
ENST00000495686.1:n.503+2793G>T
(ADAP1)
|
|
|
|
ENST00000539900.5:c.338+2793G>T
(ADAP1)
|
ENSP00000442682.1:n.338+2793G>T
|
|
|
ENST00000611167.4:c.89+2793G>T
(ADAP1)
|
ENSP00000481154.1:n.89+2793G>T
|
|
|
NM_001284308.1:c.338+2793G>T
(ADAP1)
|
NP_001271237.1:n.338+2793G>T
|
|
|
NM_001284309.1:c.89+2793G>T
(ADAP1)
|
NP_001271238.1:n.89+2793G>T
|
|
|
NM_001284310.1:c.89+2793G>T
(ADAP1)
|
NP_001271239.1:n.89+2793G>T
|
|
|
NM_006869.3:c.305+2793G>T
(ADAP1)
|
NP_006860.1:n.305+2793G>T
|
|
|
NM_006869.4:c.305+2793G>T
(ADAP1)
MANE Select
|
NP_006860.2:n.305+2793G>T
|
|
|
NM_001284309.2:c.89+2793G>T
(ADAP1)
|
NP_001271238.2:n.89+2793G>T
|
|
|
NM_001284308.2:c.338+2793G>T
(ADAP1)
|
NP_001271237.2:n.338+2793G>T
|
|
|
NM_001284310.2:c.89+2793G>T
(ADAP1)
|
NP_001271239.2:n.89+2793G>T
|
|
