NM_000170.3:c.2569+296C>T
MANE Select
|
NP_000161.2:n.2569+296C>T
|
ENST00000321612.8:c.2569+296C>T
MANE Select
|
ENSP00000370737.4:n.2569+296C>T
|
NM_000170.2:c.2569+296C>T , LRG_643t1:c.2569+296C>T
|
NP_000161.2:n.2569+296C>T
|
ENST00000321612.6:c.2569+296C>T
|
ENSP00000370737.3:n.2569+296C>T
|
ENST00000638233.1:n.1004+296C>T
|
|
ENST00000638661.1:c.769+296C>T
|
ENSP00000491369.1:n.769+296C>T
|
ENST00000638694.1:n.756+296C>T
|
|
ENST00000639318.1:c.769+296C>T
|
ENSP00000491932.1:n.769+296C>T
|
ENST00000639364.1:n.2269+296C>T
|
|
ENST00000639443.1:n.2137+296C>T
|
|
ENST00000639639.1:c.271+296C>T
|
ENSP00000491312.1:n.271+296C>T
|
ENST00000639954.1:n.2277+296C>T
|
|
ENST00000640505.1:n.808+296C>T
|
|