ENST00000460843.6:c.2628C>T
MANE Select
|
ENSP00000417980.1:p.Pro876=
|
|
ENST00000636027.1:c.2514C>T
|
ENSP00000489961.1:p.Pro838=
|
|
ENST00000637161.1:c.2535C>T
|
ENSP00000490328.1:p.Pro845=
|
|
ENST00000637261.1:c.2668C>T
|
ENSP00000490815.1:n.2668C>T
|
|
ENST00000637891.1:c.522C>T
|
ENSP00000490907.1:p.Pro174=
|
|
ENST00000637949.1:c.306C>T
|
ENSP00000489786.1:p.Pro102=
|
|
ENST00000460843.5:c.2628C>T
|
ENSP00000417980.1:p.Pro876=
|
|
ENST00000462942.3:c.1485C>T
|
ENSP00000436107.1:p.Pro495=
|
|
ENST00000482340.5:c.198C>T
|
ENSP00000486748.1:p.Pro66=
|
|
ENST00000486164.5:c.206C>T
|
|
|
ENST00000488242.2:n.154C>T
|
|
|
ENST00000493484.5:c.198C>T
|
ENSP00000486503.1:p.Pro66=
|
|
NM_024757.4:c.2628C>T
|
NP_079033.4:p.Pro876=
|
|
XM_005266105.3:c.2619C>T
|
XP_005266162.1:p.Pro873=
|
|
XM_005266110.1:c.2535C>T
|
XP_005266167.1:p.Pro845=
|
|
XM_006717288.2:c.2610C>T
|
XP_006717351.1:p.Pro870=
|
|
XM_011519021.1:c.2637C>T
|
XP_011517323.1:p.Pro879=
|
|
XM_011519022.1:c.2634C>T
|
XP_011517324.1:p.Pro878=
|
|
XM_011519023.1:c.2616C>T
|
XP_011517325.1:p.Pro872=
|
|
XM_011519024.1:c.2559C>T
|
XP_011517326.1:p.Pro853=
|
|
XM_011519025.1:c.2535C>T
|
XP_011517327.1:p.Pro845=
|
|
XM_011519026.1:c.2493C>T
|
XP_011517328.1:p.Pro831=
|
|
XM_011519027.1:c.2637C>T
|
XP_011517329.1:p.Pro879=
|
|
XM_011519029.1:c.1059C>T
|
XP_011517331.1:p.Pro353=
|
|
XM_011519030.1:c.411C>T
|
XP_011517332.1:p.Pro137=
|
|
XM_011519031.1:c.198C>T
|
XP_011517333.1:p.Pro66=
|
|
XM_011519032.1:c.198C>T
|
XP_011517334.1:p.Pro66=
|
|
XM_011519033.1:c.2472C>T
|
XP_011517335.1:p.Pro824=
|
|
NM_001354263.1:c.2607C>T
|
NP_001341192.1:p.Pro869=
|
|
XM_005266105.5:c.2619C>T
|
XP_005266162.1:p.Pro873=
|
|
XM_011519021.3:c.2637C>T
|
XP_011517323.1:p.Pro879=
|
|
XM_011519022.3:c.2634C>T
|
XP_011517324.1:p.Pro878=
|
|
XM_011519023.3:c.2616C>T
|
XP_011517325.1:p.Pro872=
|
|
XM_011519029.3:c.1059C>T
|
XP_011517331.1:p.Pro353=
|
|
XM_011519030.3:c.411C>T
|
XP_011517332.1:p.Pro137=
|
|
XM_017015134.1:c.2613C>T
|
XP_016870623.1:p.Pro871=
|
|
XM_017015136.2:c.2529C>T
|
XP_016870625.1:p.Pro843=
|
|
XM_017015137.1:c.2514C>T
|
XP_016870626.1:p.Pro838=
|
|
XM_017015138.1:c.2514C>T
|
XP_016870627.1:p.Pro838=
|
|
XM_024447674.1:c.2457C>T
|
XP_024303442.1:p.Pro819=
|
|
XM_024447675.1:c.2391C>T
|
XP_024303443.1:p.Pro797=
|
|
XM_024447676.1:c.1752C>T
|
XP_024303444.1:p.Pro584=
|
|
XM_024447677.1:c.1752C>T
|
XP_024303445.1:p.Pro584=
|
|
XM_024447678.1:c.2535C>T
|
XP_024303446.1:p.Pro845=
|
|
XM_024447680.1:c.2370C>T
|
XP_024303448.1:p.Pro790=
|
|
NM_024757.5:c.2628C>T
MANE Select
|
NP_079033.4:p.Pro876=
|
|
NM_001354263.2:c.2607C>T
|
NP_001341192.1:p.Pro869=
|
|