ENST00000298171.7:c.1831C>G
MANE Select
|
ENSP00000298171.2:p.Pro611Ala
|
|
ENST00000637447.1:c.734C>G
|
|
|
ENST00000298171.6:c.1831C>G
|
ENSP00000298171.2:p.Pro611Ala
|
|
ENST00000541158.6:c.1831C>G
|
ENSP00000441235.2:p.Pro611Ala
|
|
NM_000369.2:c.1831C>G , LRG_523t1:c.1831C>G
|
NP_000360.2:p.Pro611Ala
|
|
XM_005268037.3:c.1831C>G
|
XP_005268094.1:p.Pro611Ala
|
|
XM_011537119.1:c.1552C>G
|
XP_011535421.1:p.Pro518Ala
|
|
XR_245790.3:n.2086+21304G>C
|
|
|
XR_429385.2:n.853+21304G>C
|
|
|
XR_429386.2:n.854+21304G>C
|
|
|
XR_944075.1:n.865+21304G>C
|
|
|
XR_944076.1:n.861+21304G>C
|
|
|
XR_944077.1:n.865+21304G>C
|
|
|
XR_944078.1:n.865+21304G>C
|
|
|
XR_944079.1:n.855+21304G>C
|
|
|
XM_005268037.4:c.1831C>G
|
XP_005268094.1:p.Pro611Ala
|
|
XM_011537119.2:c.1552C>G
|
XP_011535421.1:p.Pro518Ala
|
|
XR_001751021.1:n.2753+21304G>C
|
|
|
XR_001751022.1:n.2753+21304G>C
|
|
|
XR_001751023.1:n.2753+21304G>C
|
|
|
XR_944075.3:n.929+21304G>C
|
|
|
NM_000369.4:c.1831C>G
|
NP_000360.2:p.Pro611Ala
|
|
NM_000369.5:c.1831C>G
MANE Select
|
NP_000360.2:p.Pro611Ala
|
|