ENST00000460843.6:c.3024G>C
MANE Select
|
ENSP00000417980.1:p.Arg1008Ser
|
|
ENST00000636027.1:c.2910G>C
|
ENSP00000489961.1:p.Arg970Ser
|
|
ENST00000637161.1:c.2931G>C
|
ENSP00000490328.1:p.Arg977Ser
|
|
ENST00000637261.1:c.3064G>C
|
ENSP00000490815.1:n.3064G>C
|
|
ENST00000637891.1:c.918G>C
|
ENSP00000490907.1:p.Arg306Ser
|
|
ENST00000460843.5:c.3024G>C
|
ENSP00000417980.1:p.Arg1008Ser
|
|
ENST00000462942.3:c.1881G>C
|
ENSP00000436107.1:p.Arg627Ser
|
|
ENST00000486164.5:c.711G>C
|
|
|
ENST00000488242.2:n.550G>C
|
|
|
NM_024757.4:c.3024G>C
|
NP_079033.4:p.Arg1008Ser
|
|
XM_005266105.3:c.3015G>C
|
XP_005266162.1:p.Arg1005Ser
|
|
XM_005266110.1:c.2931G>C
|
XP_005266167.1:p.Arg977Ser
|
|
XM_006717288.2:c.3006G>C
|
XP_006717351.1:p.Arg1002Ser
|
|
XM_011519021.1:c.3033G>C
|
XP_011517323.1:p.Arg1011Ser
|
|
XM_011519022.1:c.3030G>C
|
XP_011517324.1:p.Arg1010Ser
|
|
XM_011519023.1:c.3012G>C
|
XP_011517325.1:p.Arg1004Ser
|
|
XM_011519024.1:c.2955G>C
|
XP_011517326.1:p.Arg985Ser
|
|
XM_011519025.1:c.2931G>C
|
XP_011517327.1:p.Arg977Ser
|
|
XM_011519026.1:c.2889G>C
|
XP_011517328.1:p.Arg963Ser
|
|
XM_011519029.1:c.1455G>C
|
XP_011517331.1:p.Arg485Ser
|
|
XM_011519030.1:c.807G>C
|
XP_011517332.1:p.Arg269Ser
|
|
XM_011519031.1:c.594G>C
|
XP_011517333.1:p.Arg198Ser
|
|
XM_011519032.1:c.594G>C
|
XP_011517334.1:p.Arg198Ser
|
|
XM_011519033.1:c.2868G>C
|
XP_011517335.1:p.Arg956Ser
|
|
NM_001354263.1:c.3003G>C
|
NP_001341192.1:p.Arg1001Ser
|
|
XM_005266105.5:c.3015G>C
|
XP_005266162.1:p.Arg1005Ser
|
|
XM_011519021.3:c.3033G>C
|
XP_011517323.1:p.Arg1011Ser
|
|
XM_011519022.3:c.3030G>C
|
XP_011517324.1:p.Arg1010Ser
|
|
XM_011519023.3:c.3012G>C
|
XP_011517325.1:p.Arg1004Ser
|
|
XM_011519029.3:c.1455G>C
|
XP_011517331.1:p.Arg485Ser
|
|
XM_011519030.3:c.807G>C
|
XP_011517332.1:p.Arg269Ser
|
|
XM_017015134.1:c.3009G>C
|
XP_016870623.1:p.Arg1003Ser
|
|
XM_017015136.2:c.2925G>C
|
XP_016870625.1:p.Arg975Ser
|
|
XM_017015137.1:c.2910G>C
|
XP_016870626.1:p.Arg970Ser
|
|
XM_017015138.1:c.2910G>C
|
XP_016870627.1:p.Arg970Ser
|
|
XM_024447674.1:c.2853G>C
|
XP_024303442.1:p.Arg951Ser
|
|
XM_024447675.1:c.2787G>C
|
XP_024303443.1:p.Arg929Ser
|
|
XM_024447676.1:c.2148G>C
|
XP_024303444.1:p.Arg716Ser
|
|
XM_024447677.1:c.2148G>C
|
XP_024303445.1:p.Arg716Ser
|
|
XM_024447680.1:c.2766G>C
|
XP_024303448.1:p.Arg922Ser
|
|
NM_024757.5:c.3024G>C
MANE Select
|
NP_079033.4:p.Arg1008Ser
|
|
NM_001354263.2:c.3003G>C
|
NP_001341192.1:p.Arg1001Ser
|
|