ENST00000642496.1:c.4044C>T
|
|
|
ENST00000644397.2:c.5185C>T
MANE Select
|
ENSP00000495195.1:p.Pro1729Ser
|
|
ENST00000373965.6:c.4996C>T
|
ENSP00000363076.3:p.Pro1666Ser
|
|
ENST00000414778.5:c.4993C>T
|
ENSP00000410304.2:p.Pro1665Ser
|
|
ENST00000495484.5:c.1213C>T
|
ENSP00000480780.1:p.Pro405Ser
|
|
ENST00000614895.4:c.5008C>T
|
ENSP00000478512.1:p.Pro1670Ser
|
|
ENST00000616114.4:c.4990C>T
|
ENSP00000483745.1:p.Pro1664Ser
|
|
ENST00000618301.4:c.1345C>T
|
ENSP00000482780.1:p.Pro449Ser
|
|
ENST00000621708.4:c.5011C>T
|
ENSP00000484454.1:p.Pro1671Ser
|
|
NM_001142771.1:c.5011C>T
|
NP_001136243.1:p.Pro1671Ser
|
|
NM_001142772.1:c.4996C>T
|
NP_001136244.1:p.Pro1666Ser
|
|
NM_001354420.1:c.4990C>T
|
NP_001341349.1:p.Pro1664Ser
|
|
NM_001354429.1:c.5119C>T
|
NP_001341358.1:p.Pro1707Ser
|
|
XR_001747192.2:n.11477C>T
|
|
|
XR_001747193.2:n.11468C>T
|
|
|
NM_001142771.2:c.5011C>T
|
NP_001136243.1:p.Pro1671Ser
|
|
NM_001142772.2:c.4996C>T
|
NP_001136244.1:p.Pro1666Ser
|
|
NM_001354420.2:c.4990C>T
|
NP_001341349.1:p.Pro1664Ser
|
|
NM_001354429.2:c.5119C>T
|
NP_001341358.1:p.Pro1707Ser
|
|
NM_001384140.1:c.5185C>T
MANE Select
|
NP_001371069.1:p.Pro1729Ser
|
|