ENST00000696170.1:c.*661-29G>T
|
ENSP00000512461.1:n.*661-29G>T
|
|
ENST00000696171.1:c.1056-29G>T
|
ENSP00000512462.1:n.1056-29G>T
|
|
ENST00000378588.5:c.1152-29G>T
MANE Select
|
ENSP00000367851.4:n.1152-29G>T
|
|
ENST00000378588.4:c.1152-29G>T
|
ENSP00000367851.4:n.1152-29G>T
|
|
ENST00000465127.1:c.171+378977G>T
|
ENSP00000417050.1:n.171+378977G>T
|
|
NM_000397.3:c.1152-29G>T , LRG_53t1:c.1152-29G>T
|
NP_000388.2:n.1152-29G>T
|
|
XM_011543890.1:c.846-29G>T
|
XP_011542192.1:n.846-29G>T
|
|
NM_000397.4:c.1152-29G>T
MANE Select
|
NP_000388.2:n.1152-29G>T
|
|