ENST00000460843.6:c.2897C>A
MANE Select
|
ENSP00000417980.1:p.Thr966Asn
|
|
ENST00000636027.1:c.2783C>A
|
ENSP00000489961.1:p.Thr928Asn
|
|
ENST00000637161.1:c.2804C>A
|
ENSP00000490328.1:p.Thr935Asn
|
|
ENST00000637261.1:c.2937C>A
|
ENSP00000490815.1:n.2937C>A
|
|
ENST00000637891.1:c.791C>A
|
ENSP00000490907.1:p.Thr264Asn
|
|
ENST00000460843.5:c.2897C>A
|
ENSP00000417980.1:p.Thr966Asn
|
|
ENST00000462942.3:c.1754C>A
|
ENSP00000436107.1:p.Thr585Asn
|
|
ENST00000486164.5:c.584C>A
|
|
|
ENST00000488242.2:n.423C>A
|
|
|
NM_024757.4:c.2897C>A
|
NP_079033.4:p.Thr966Asn
|
|
XM_005266105.3:c.2888C>A
|
XP_005266162.1:p.Thr963Asn
|
|
XM_005266110.1:c.2804C>A
|
XP_005266167.1:p.Thr935Asn
|
|
XM_006717288.2:c.2879C>A
|
XP_006717351.1:p.Thr960Asn
|
|
XM_011519021.1:c.2906C>A
|
XP_011517323.1:p.Thr969Asn
|
|
XM_011519022.1:c.2903C>A
|
XP_011517324.1:p.Thr968Asn
|
|
XM_011519023.1:c.2885C>A
|
XP_011517325.1:p.Thr962Asn
|
|
XM_011519024.1:c.2828C>A
|
XP_011517326.1:p.Thr943Asn
|
|
XM_011519025.1:c.2804C>A
|
XP_011517327.1:p.Thr935Asn
|
|
XM_011519026.1:c.2762C>A
|
XP_011517328.1:p.Thr921Asn
|
|
XM_011519029.1:c.1328C>A
|
XP_011517331.1:p.Thr443Asn
|
|
XM_011519030.1:c.680C>A
|
XP_011517332.1:p.Thr227Asn
|
|
XM_011519031.1:c.467C>A
|
XP_011517333.1:p.Thr156Asn
|
|
XM_011519032.1:c.467C>A
|
XP_011517334.1:p.Thr156Asn
|
|
XM_011519033.1:c.2741C>A
|
XP_011517335.1:p.Thr914Asn
|
|
NM_001354263.1:c.2876C>A
|
NP_001341192.1:p.Thr959Asn
|
|
XM_005266105.5:c.2888C>A
|
XP_005266162.1:p.Thr963Asn
|
|
XM_011519021.3:c.2906C>A
|
XP_011517323.1:p.Thr969Asn
|
|
XM_011519022.3:c.2903C>A
|
XP_011517324.1:p.Thr968Asn
|
|
XM_011519023.3:c.2885C>A
|
XP_011517325.1:p.Thr962Asn
|
|
XM_011519029.3:c.1328C>A
|
XP_011517331.1:p.Thr443Asn
|
|
XM_011519030.3:c.680C>A
|
XP_011517332.1:p.Thr227Asn
|
|
XM_017015134.1:c.2882C>A
|
XP_016870623.1:p.Thr961Asn
|
|
XM_017015136.2:c.2798C>A
|
XP_016870625.1:p.Thr933Asn
|
|
XM_017015137.1:c.2783C>A
|
XP_016870626.1:p.Thr928Asn
|
|
XM_017015138.1:c.2783C>A
|
XP_016870627.1:p.Thr928Asn
|
|
XM_024447674.1:c.2726C>A
|
XP_024303442.1:p.Thr909Asn
|
|
XM_024447675.1:c.2660C>A
|
XP_024303443.1:p.Thr887Asn
|
|
XM_024447676.1:c.2021C>A
|
XP_024303444.1:p.Thr674Asn
|
|
XM_024447677.1:c.2021C>A
|
XP_024303445.1:p.Thr674Asn
|
|
XM_024447680.1:c.2639C>A
|
XP_024303448.1:p.Thr880Asn
|
|
NM_024757.5:c.2897C>A
MANE Select
|
NP_079033.4:p.Thr966Asn
|
|
NM_001354263.2:c.2876C>A
|
NP_001341192.1:p.Thr959Asn
|
|