ENST00000367400.8:c.4043T>C
MANE Select
|
ENSP00000356370.3:p.Ile1348Thr
|
|
ENST00000367399.6:c.3707T>C
|
ENSP00000356369.2:p.Ile1236Thr
|
|
ENST00000367400.7:c.4043T>C
|
ENSP00000356370.3:p.Ile1348Thr
|
|
ENST00000448952.1:c.277T>C
|
ENSP00000395407.1:n.277T>C
|
|
ENST00000484075.5:c.*154T>C
|
ENSP00000433932.1:n.*154T>C
|
|
ENST00000535699.5:c.3971T>C
|
ENSP00000438786.1:p.Ile1324Thr
|
|
ENST00000538660.5:c.2435T>C
|
ENSP00000438091.1:p.Ile812Thr
|
|
NM_001193640.1:c.3707T>C
|
NP_001180569.1:p.Ile1236Thr
|
|
NM_001257965.1:c.3971T>C
|
NP_001244894.1:p.Ile1324Thr
|
|
NM_001257966.1:c.2435T>C
|
NP_001244895.1:p.Ile812Thr
|
|
NM_201253.2:c.4043T>C
|
NP_957705.1:p.Ile1348Thr
|
|
NR_047563.1:n.4044T>C
|
|
|
NR_047564.1:n.4494T>C
|
|
|
XM_011509366.1:c.*148T>C
|
XP_011507668.1:n.*148T>C
|
|
XM_011509367.1:c.*22T>C
|
XP_011507669.1:n.*22T>C
|
|
XM_011509368.1:c.3461T>C
|
XP_011507670.1:p.Ile1154Thr
|
|
XM_011509369.1:c.2486T>C
|
XP_011507671.1:p.Ile829Thr
|
|
XM_011509369.2:c.2486T>C
|
XP_011507671.1:p.Ile829Thr
|
|
XM_017000851.1:c.3200T>C
|
XP_016856340.1:p.Ile1067Thr
|
|
XM_017000852.1:c.4178T>C
|
XP_016856341.1:p.Ile1393Thr
|
|
NM_201253.3:c.4043T>C
MANE Select
|
NP_957705.1:p.Ile1348Thr
|
|
NM_001193640.2:c.3707T>C
|
NP_001180569.1:p.Ile1236Thr
|
|
NM_001257965.2:c.3971T>C
|
NP_001244894.1:p.Ile1324Thr
|
|
NR_047563.2:n.3996T>C
|
|
|
NR_047564.2:n.4446T>C
|
|
|
NM_001257966.2:c.2435T>C
|
NP_001244895.1:p.Ile812Thr
|
|