ENST00000706989.1:c.2482T>A
|
ENSP00000516702.1:p.Ser828Thr
|
|
ENST00000359125.7:c.2428T>A
MANE Select
|
ENSP00000352035.2:p.Ser810Thr
|
|
ENST00000637193.1:c.1825T>A
|
ENSP00000490734.1:p.Ser609Thr
|
|
ENST00000344462.8:c.2335T>A
|
ENSP00000339611.4:p.Ser779Thr
|
|
ENST00000357249.6:c.1996T>A
|
ENSP00000349789.3:p.Ser666Thr
|
|
ENST00000359125.6:c.2428T>A
|
ENSP00000352035.2:p.Ser810Thr
|
|
ENST00000360480.7:c.2344T>A
|
ENSP00000353668.3:p.Ser782Thr
|
|
ENST00000370224.5:c.2241+211T>A
|
ENSP00000359244.2:n.2241+211T>A
|
|
ENST00000625514.2:c.2205+211T>A
|
ENSP00000486040.1:n.2205+211T>A
|
|
ENST00000626839.2:c.2374T>A
|
ENSP00000486706.1:p.Ser792Thr
|
|
ENST00000629241.2:c.2133+211T>A
|
ENSP00000487142.1:n.2133+211T>A
|
|
ENST00000629676.2:c.1680-5992T>A
|
ENSP00000486194.1:n.1680-5992T>A
|
|
NM_004518.4:c.2344T>A
|
NP_004509.2:p.Ser782Thr
|
|
NM_172106.1:c.2374T>A
|
NP_742104.1:p.Ser792Thr
|
|
NM_172107.2:c.2428T>A
|
NP_742105.1:p.Ser810Thr
|
|
NM_172108.3:c.2335T>A
|
NP_742106.1:p.Ser779Thr
|
|
XM_006723787.1:c.2470T>A
|
XP_006723850.1:p.Ser824Thr
|
|
XM_011528807.1:c.2536T>A
|
XP_011527109.1:p.Ser846Thr
|
|
XM_011528808.1:c.2533T>A
|
XP_011527110.1:p.Ser845Thr
|
|
XM_011528809.1:c.2506T>A
|
XP_011527111.1:p.Ser836Thr
|
|
XM_011528810.1:c.2482T>A
|
XP_011527112.1:p.Ser828Thr
|
|
XM_011528811.1:c.2452T>A
|
XP_011527113.1:p.Ser818Thr
|
|
XM_011528812.1:c.2425T>A
|
XP_011527114.1:p.Ser809Thr
|
|
XM_011528813.1:c.2410T>A
|
XP_011527115.1:p.Ser804Thr
|
|
XM_011528814.1:c.2017T>A
|
XP_011527116.1:p.Ser673Thr
|
|
NM_004518.5:c.2344T>A
|
NP_004509.2:p.Ser782Thr
|
|
NM_172106.2:c.2374T>A
|
NP_742104.1:p.Ser792Thr
|
|
NM_172107.3:c.2428T>A
|
NP_742105.1:p.Ser810Thr
|
|
NM_172108.4:c.2335T>A
|
NP_742106.1:p.Ser779Thr
|
|
XM_011528810.2:c.2482T>A
|
XP_011527112.1:p.Ser828Thr
|
|
XM_011528811.2:c.2452T>A
|
XP_011527113.1:p.Ser818Thr
|
|
XM_017027841.2:c.2479T>A
|
XP_016883330.1:p.Ser827Thr
|
|
XM_017027842.2:c.2416T>A
|
XP_016883331.1:p.Ser806Thr
|
|
XM_017027843.1:c.2413T>A
|
XP_016883332.1:p.Ser805Thr
|
|
XM_017027844.2:c.2371T>A
|
XP_016883333.1:p.Ser791Thr
|
|
XM_017027845.1:c.1444T>A
|
XP_016883334.1:p.Ser482Thr
|
|
NM_004518.6:c.2344T>A
|
NP_004509.2:p.Ser782Thr
|
|
NM_172106.3:c.2374T>A
|
NP_742104.1:p.Ser792Thr
|
|
NM_172107.4:c.2428T>A
MANE Select
|
NP_742105.1:p.Ser810Thr
|
|
NM_172108.5:c.2335T>A
|
NP_742106.1:p.Ser779Thr
|
|
NM_001382235.1:c.2482T>A
|
NP_001369164.1:p.Ser828Thr
|
|