NM_000097.7:c.1278-6G>T
MANE Select
|
NP_000088.3:n.1278-6G>T
|
ENST00000647941.2:c.1278-6G>T
MANE Select
|
ENSP00000497326.1:n.1278-6G>T
|
NM_000097.5:c.1278-6G>T
|
NP_000088.3:n.1278-6G>T
|
ENST00000264193.2:c.1278-6G>T
|
ENSP00000264193.2:n.1278-6G>T
|
ENST00000512905.5:c.163+631G>T
|
|
ENST00000512905.6:c.163+631G>T
|
|
XM_005247125.3:c.1173-2506G>T
|
XP_005247182.1:n.1173-2506G>T
|
XM_005247125.4:c.1173-2506G>T
|
XP_005247182.1:n.1173-2506G>T
|
XR_001740025.2:n.1344-2506G>T
|
|
XR_001740026.1:n.2013-6G>T
|
|
XR_001740027.1:n.1553-6G>T
|
|
XR_001740028.1:n.1519-6G>T
|
|