ENST00000460843.6:c.2904G>C
MANE Select
|
ENSP00000417980.1:p.Lys968Asn
|
|
ENST00000636027.1:c.2790G>C
|
ENSP00000489961.1:p.Lys930Asn
|
|
ENST00000637161.1:c.2811G>C
|
ENSP00000490328.1:p.Lys937Asn
|
|
ENST00000637261.1:c.2944G>C
|
ENSP00000490815.1:n.2944G>C
|
|
ENST00000637891.1:c.798G>C
|
ENSP00000490907.1:p.Lys266Asn
|
|
ENST00000460843.5:c.2904G>C
|
ENSP00000417980.1:p.Lys968Asn
|
|
ENST00000462942.3:c.1761G>C
|
ENSP00000436107.1:p.Lys587Asn
|
|
ENST00000486164.5:c.591G>C
|
|
|
ENST00000488242.2:n.430G>C
|
|
|
NM_024757.4:c.2904G>C
|
NP_079033.4:p.Lys968Asn
|
|
XM_005266105.3:c.2895G>C
|
XP_005266162.1:p.Lys965Asn
|
|
XM_005266110.1:c.2811G>C
|
XP_005266167.1:p.Lys937Asn
|
|
XM_006717288.2:c.2886G>C
|
XP_006717351.1:p.Lys962Asn
|
|
XM_011519021.1:c.2913G>C
|
XP_011517323.1:p.Lys971Asn
|
|
XM_011519022.1:c.2910G>C
|
XP_011517324.1:p.Lys970Asn
|
|
XM_011519023.1:c.2892G>C
|
XP_011517325.1:p.Lys964Asn
|
|
XM_011519024.1:c.2835G>C
|
XP_011517326.1:p.Lys945Asn
|
|
XM_011519025.1:c.2811G>C
|
XP_011517327.1:p.Lys937Asn
|
|
XM_011519026.1:c.2769G>C
|
XP_011517328.1:p.Lys923Asn
|
|
XM_011519029.1:c.1335G>C
|
XP_011517331.1:p.Lys445Asn
|
|
XM_011519030.1:c.687G>C
|
XP_011517332.1:p.Lys229Asn
|
|
XM_011519031.1:c.474G>C
|
XP_011517333.1:p.Lys158Asn
|
|
XM_011519032.1:c.474G>C
|
XP_011517334.1:p.Lys158Asn
|
|
XM_011519033.1:c.2748G>C
|
XP_011517335.1:p.Lys916Asn
|
|
NM_001354263.1:c.2883G>C
|
NP_001341192.1:p.Lys961Asn
|
|
XM_005266105.5:c.2895G>C
|
XP_005266162.1:p.Lys965Asn
|
|
XM_011519021.3:c.2913G>C
|
XP_011517323.1:p.Lys971Asn
|
|
XM_011519022.3:c.2910G>C
|
XP_011517324.1:p.Lys970Asn
|
|
XM_011519023.3:c.2892G>C
|
XP_011517325.1:p.Lys964Asn
|
|
XM_011519029.3:c.1335G>C
|
XP_011517331.1:p.Lys445Asn
|
|
XM_011519030.3:c.687G>C
|
XP_011517332.1:p.Lys229Asn
|
|
XM_017015134.1:c.2889G>C
|
XP_016870623.1:p.Lys963Asn
|
|
XM_017015136.2:c.2805G>C
|
XP_016870625.1:p.Lys935Asn
|
|
XM_017015137.1:c.2790G>C
|
XP_016870626.1:p.Lys930Asn
|
|
XM_017015138.1:c.2790G>C
|
XP_016870627.1:p.Lys930Asn
|
|
XM_024447674.1:c.2733G>C
|
XP_024303442.1:p.Lys911Asn
|
|
XM_024447675.1:c.2667G>C
|
XP_024303443.1:p.Lys889Asn
|
|
XM_024447676.1:c.2028G>C
|
XP_024303444.1:p.Lys676Asn
|
|
XM_024447677.1:c.2028G>C
|
XP_024303445.1:p.Lys676Asn
|
|
XM_024447680.1:c.2646G>C
|
XP_024303448.1:p.Lys882Asn
|
|
NM_024757.5:c.2904G>C
MANE Select
|
NP_079033.4:p.Lys968Asn
|
|
NM_001354263.2:c.2883G>C
|
NP_001341192.1:p.Lys961Asn
|
|