ENST00000460843.6:c.3014C>G
MANE Select
|
ENSP00000417980.1:p.Pro1005Arg
|
|
ENST00000636027.1:c.2900C>G
|
ENSP00000489961.1:p.Pro967Arg
|
|
ENST00000637161.1:c.2921C>G
|
ENSP00000490328.1:p.Pro974Arg
|
|
ENST00000637261.1:c.3054C>G
|
ENSP00000490815.1:n.3054C>G
|
|
ENST00000637891.1:c.908C>G
|
ENSP00000490907.1:p.Pro303Arg
|
|
ENST00000460843.5:c.3014C>G
|
ENSP00000417980.1:p.Pro1005Arg
|
|
ENST00000462942.3:c.1871C>G
|
ENSP00000436107.1:p.Pro624Arg
|
|
ENST00000486164.5:c.701C>G
|
|
|
ENST00000488242.2:n.540C>G
|
|
|
NM_024757.4:c.3014C>G
|
NP_079033.4:p.Pro1005Arg
|
|
XM_005266105.3:c.3005C>G
|
XP_005266162.1:p.Pro1002Arg
|
|
XM_005266110.1:c.2921C>G
|
XP_005266167.1:p.Pro974Arg
|
|
XM_006717288.2:c.2996C>G
|
XP_006717351.1:p.Pro999Arg
|
|
XM_011519021.1:c.3023C>G
|
XP_011517323.1:p.Pro1008Arg
|
|
XM_011519022.1:c.3020C>G
|
XP_011517324.1:p.Pro1007Arg
|
|
XM_011519023.1:c.3002C>G
|
XP_011517325.1:p.Pro1001Arg
|
|
XM_011519024.1:c.2945C>G
|
XP_011517326.1:p.Pro982Arg
|
|
XM_011519025.1:c.2921C>G
|
XP_011517327.1:p.Pro974Arg
|
|
XM_011519026.1:c.2879C>G
|
XP_011517328.1:p.Pro960Arg
|
|
XM_011519029.1:c.1445C>G
|
XP_011517331.1:p.Pro482Arg
|
|
XM_011519030.1:c.797C>G
|
XP_011517332.1:p.Pro266Arg
|
|
XM_011519031.1:c.584C>G
|
XP_011517333.1:p.Pro195Arg
|
|
XM_011519032.1:c.584C>G
|
XP_011517334.1:p.Pro195Arg
|
|
XM_011519033.1:c.2858C>G
|
XP_011517335.1:p.Pro953Arg
|
|
NM_001354263.1:c.2993C>G
|
NP_001341192.1:p.Pro998Arg
|
|
XM_005266105.5:c.3005C>G
|
XP_005266162.1:p.Pro1002Arg
|
|
XM_011519021.3:c.3023C>G
|
XP_011517323.1:p.Pro1008Arg
|
|
XM_011519022.3:c.3020C>G
|
XP_011517324.1:p.Pro1007Arg
|
|
XM_011519023.3:c.3002C>G
|
XP_011517325.1:p.Pro1001Arg
|
|
XM_011519029.3:c.1445C>G
|
XP_011517331.1:p.Pro482Arg
|
|
XM_011519030.3:c.797C>G
|
XP_011517332.1:p.Pro266Arg
|
|
XM_017015134.1:c.2999C>G
|
XP_016870623.1:p.Pro1000Arg
|
|
XM_017015136.2:c.2915C>G
|
XP_016870625.1:p.Pro972Arg
|
|
XM_017015137.1:c.2900C>G
|
XP_016870626.1:p.Pro967Arg
|
|
XM_017015138.1:c.2900C>G
|
XP_016870627.1:p.Pro967Arg
|
|
XM_024447674.1:c.2843C>G
|
XP_024303442.1:p.Pro948Arg
|
|
XM_024447675.1:c.2777C>G
|
XP_024303443.1:p.Pro926Arg
|
|
XM_024447676.1:c.2138C>G
|
XP_024303444.1:p.Pro713Arg
|
|
XM_024447677.1:c.2138C>G
|
XP_024303445.1:p.Pro713Arg
|
|
XM_024447680.1:c.2756C>G
|
XP_024303448.1:p.Pro919Arg
|
|
NM_024757.5:c.3014C>G
MANE Select
|
NP_079033.4:p.Pro1005Arg
|
|
NM_001354263.2:c.2993C>G
|
NP_001341192.1:p.Pro998Arg
|
|