ENST00000294304.12:c.4490T>C
MANE Select
|
ENSP00000294304.6:p.Ile1497Thr
|
|
ENST00000294304.11:c.4490T>C
|
ENSP00000294304.6:p.Ile1497Thr
|
|
ENST00000529702.1:c.160T>C
|
|
|
ENST00000529993.5:c.*3096T>C
|
ENSP00000436652.1:n.*3096T>C
|
|
NM_001291902.1:c.2747T>C
|
NP_001278831.1:p.Ile916Thr
|
|
NM_002335.3:c.4490T>C
|
NP_002326.2:p.Ile1497Thr
|
|
XM_005273994.2:c.4604T>C
|
XP_005274051.1:p.Ile1535Thr
|
|
XM_011545029.1:c.4631T>C
|
XP_011543331.1:p.Ile1544Thr
|
|
XM_011545030.1:c.4517T>C
|
XP_011543332.1:p.Ile1506Thr
|
|
XM_011545031.1:c.4647T>C
|
XP_011543333.1:p.Asp1549=
|
|
XR_949925.1:n.4646T>C
|
|
|
XR_949926.1:n.4662T>C
|
|
|
XM_017017735.1:c.2861T>C
|
XP_016873224.1:p.Ile954Thr
|
|
XM_017017736.1:c.2144T>C
|
XP_016873225.1:p.Ile715Thr
|
|
XR_949925.2:n.4646T>C
|
|
|
XR_949926.2:n.4662T>C
|
|
|
NM_002335.4:c.4490T>C
MANE Select
|
NP_002326.2:p.Ile1497Thr
|
|
NM_001291902.2:c.2747T>C
|
NP_001278831.1:p.Ile916Thr
|
|