ENST00000382329.2:c.3233T>C
|
ENSP00000371766.2:p.Ile1078Thr
|
|
ENST00000683406.1:n.54T>C
|
|
|
ENST00000685949.1:n.2321T>C
|
|
|
ENST00000432829.7:c.3533T>C
MANE Select
|
ENSP00000394888.3:p.Ile1178Thr
|
|
ENST00000382329.1:c.1934T>C
|
ENSP00000371766.1:p.Ile645Thr
|
|
ENST00000432829.6:c.3533T>C
|
ENSP00000394888.3:p.Ile1178Thr
|
|
ENST00000453981.5:c.3329T>C
|
ENSP00000408464.2:p.Ile1110Thr
|
|
ENST00000469391.5:c.3233T>C
|
ENSP00000419438.1:p.Ile1078Thr
|
|
ENST00000495184.5:n.5488T>C
|
|
|
NM_001190458.1:c.3233T>C
|
NP_001177387.1:p.Ile1078Thr
|
|
NM_001193536.1:c.3329T>C
|
NP_001180465.1:p.Ile1110Thr
|
|
NM_203447.3:c.3533T>C , LRG_196t1:c.3533T>C
|
NP_982272.2:p.Ile1178Thr
|
|
XM_011518045.1:c.3233T>C
|
XP_011516347.1:p.Ile1078Thr
|
|
XM_011518046.1:c.3395T>C
|
XP_011516348.1:p.Ile1132Thr
|
|
XM_011518047.1:c.3329T>C
|
XP_011516349.1:p.Ile1110Thr
|
|
XM_011518048.1:c.3329T>C
|
XP_011516350.1:p.Ile1110Thr
|
|
XM_011518049.1:c.1769T>C
|
XP_011516351.1:p.Ile590Thr
|
|
XM_011518045.3:c.3233T>C
|
XP_011516347.1:p.Ile1078Thr
|
|
XM_011518046.2:c.3395T>C
|
XP_011516348.1:p.Ile1132Thr
|
|
XM_011518047.3:c.3329T>C
|
XP_011516349.1:p.Ile1110Thr
|
|
XM_011518048.2:c.3329T>C
|
XP_011516350.1:p.Ile1110Thr
|
|
XM_011518049.2:c.1769T>C
|
XP_011516351.1:p.Ile590Thr
|
|
XM_017015173.1:c.3329T>C
|
XP_016870662.1:p.Ile1110Thr
|
|
XM_017015174.1:c.3395T>C
|
XP_016870663.1:p.Ile1132Thr
|
|
NM_001190458.2:c.3233T>C
|
NP_001177387.1:p.Ile1078Thr
|
|
NM_001193536.2:c.3329T>C
|
NP_001180465.1:p.Ile1110Thr
|
|
NM_203447.4:c.3533T>C
MANE Select
|
NP_982272.2:p.Ile1178Thr
|
|