ENST00000696170.1:c.*39T>C
|
ENSP00000512461.1:n.*39T>C
|
|
ENST00000696171.1:c.434T>C
|
ENSP00000512462.1:p.Ile145Thr
|
|
ENST00000696172.1:c.338-2958T>C
|
ENSP00000512463.1:n.338-2958T>C
|
|
ENST00000378588.5:c.530T>C
MANE Select
|
ENSP00000367851.4:p.Ile177Thr
|
|
ENST00000378588.4:c.530T>C
|
ENSP00000367851.4:p.Ile177Thr
|
|
ENST00000465127.1:c.171+369997T>C
|
ENSP00000417050.1:n.171+369997T>C
|
|
NM_000397.3:c.530T>C , LRG_53t1:c.530T>C
|
NP_000388.2:p.Ile177Thr
|
|
XM_011543890.1:c.224T>C
|
XP_011542192.1:p.Ile75Thr
|
|
NM_000397.4:c.530T>C
MANE Select
|
NP_000388.2:p.Ile177Thr
|
|