ENST00000460843.6:c.3008C>A
MANE Select
|
ENSP00000417980.1:p.Pro1003His
|
|
ENST00000636027.1:c.2894C>A
|
ENSP00000489961.1:p.Pro965His
|
|
ENST00000637161.1:c.2915C>A
|
ENSP00000490328.1:p.Pro972His
|
|
ENST00000637261.1:c.3048C>A
|
ENSP00000490815.1:n.3048C>A
|
|
ENST00000637891.1:c.902C>A
|
ENSP00000490907.1:p.Pro301His
|
|
ENST00000460843.5:c.3008C>A
|
ENSP00000417980.1:p.Pro1003His
|
|
ENST00000462942.3:c.1865C>A
|
ENSP00000436107.1:p.Pro622His
|
|
ENST00000486164.5:c.695C>A
|
|
|
ENST00000488242.2:n.534C>A
|
|
|
NM_024757.4:c.3008C>A
|
NP_079033.4:p.Pro1003His
|
|
XM_005266105.3:c.2999C>A
|
XP_005266162.1:p.Pro1000His
|
|
XM_005266110.1:c.2915C>A
|
XP_005266167.1:p.Pro972His
|
|
XM_006717288.2:c.2990C>A
|
XP_006717351.1:p.Pro997His
|
|
XM_011519021.1:c.3017C>A
|
XP_011517323.1:p.Pro1006His
|
|
XM_011519022.1:c.3014C>A
|
XP_011517324.1:p.Pro1005His
|
|
XM_011519023.1:c.2996C>A
|
XP_011517325.1:p.Pro999His
|
|
XM_011519024.1:c.2939C>A
|
XP_011517326.1:p.Pro980His
|
|
XM_011519025.1:c.2915C>A
|
XP_011517327.1:p.Pro972His
|
|
XM_011519026.1:c.2873C>A
|
XP_011517328.1:p.Pro958His
|
|
XM_011519029.1:c.1439C>A
|
XP_011517331.1:p.Pro480His
|
|
XM_011519030.1:c.791C>A
|
XP_011517332.1:p.Pro264His
|
|
XM_011519031.1:c.578C>A
|
XP_011517333.1:p.Pro193His
|
|
XM_011519032.1:c.578C>A
|
XP_011517334.1:p.Pro193His
|
|
XM_011519033.1:c.2852C>A
|
XP_011517335.1:p.Pro951His
|
|
NM_001354263.1:c.2987C>A
|
NP_001341192.1:p.Pro996His
|
|
XM_005266105.5:c.2999C>A
|
XP_005266162.1:p.Pro1000His
|
|
XM_011519021.3:c.3017C>A
|
XP_011517323.1:p.Pro1006His
|
|
XM_011519022.3:c.3014C>A
|
XP_011517324.1:p.Pro1005His
|
|
XM_011519023.3:c.2996C>A
|
XP_011517325.1:p.Pro999His
|
|
XM_011519029.3:c.1439C>A
|
XP_011517331.1:p.Pro480His
|
|
XM_011519030.3:c.791C>A
|
XP_011517332.1:p.Pro264His
|
|
XM_017015134.1:c.2993C>A
|
XP_016870623.1:p.Pro998His
|
|
XM_017015136.2:c.2909C>A
|
XP_016870625.1:p.Pro970His
|
|
XM_017015137.1:c.2894C>A
|
XP_016870626.1:p.Pro965His
|
|
XM_017015138.1:c.2894C>A
|
XP_016870627.1:p.Pro965His
|
|
XM_024447674.1:c.2837C>A
|
XP_024303442.1:p.Pro946His
|
|
XM_024447675.1:c.2771C>A
|
XP_024303443.1:p.Pro924His
|
|
XM_024447676.1:c.2132C>A
|
XP_024303444.1:p.Pro711His
|
|
XM_024447677.1:c.2132C>A
|
XP_024303445.1:p.Pro711His
|
|
XM_024447680.1:c.2750C>A
|
XP_024303448.1:p.Pro917His
|
|
NM_024757.5:c.3008C>A
MANE Select
|
NP_079033.4:p.Pro1003His
|
|
NM_001354263.2:c.2987C>A
|
NP_001341192.1:p.Pro996His
|
|