ENST00000450053.8:c.4279G>C
MANE Select
|
ENSP00000415034.2:p.Asp1427His
|
|
ENST00000651747.1:c.4177G>C
|
ENSP00000499216.1:p.Asp1393His
|
|
ENST00000416683.5:c.2142G>C
|
|
|
ENST00000450053.7:c.4279G>C
|
ENSP00000415034.2:p.Asp1427His
|
|
NM_015175.2:c.4279G>C , LRG_568t1:c.4279G>C
|
NP_055990.1:p.Asp1427His
|
|
XM_005264992.2:c.4177G>C
|
XP_005265049.1:p.Asp1393His
|
|
XM_005264993.2:c.751G>C
|
XP_005265050.1:p.Asp251His
|
|
XM_006713072.2:c.4198G>C
|
XP_006713135.1:p.Asp1400His
|
|
XM_011533532.1:c.4258G>C
|
XP_011531834.1:p.Asp1420His
|
|
XM_011533533.1:c.4279G>C
|
XP_011531835.1:p.Asp1427His
|
|
XM_011533534.1:c.3910G>C
|
XP_011531836.1:p.Asp1304His
|
|
XM_011533535.1:c.3739G>C
|
XP_011531837.1:p.Asp1247His
|
|
XM_011533536.1:c.3625G>C
|
XP_011531838.1:p.Asp1209His
|
|
XM_011533537.1:c.3187G>C
|
XP_011531839.1:p.Asp1063His
|
|
XR_940397.1:n.4455G>C
|
|
|
XR_940398.1:n.4455G>C
|
|
|
NM_001365116.1:c.4177G>C
|
NP_001352045.1:p.Asp1393His
|
|
XM_006713072.3:c.4198G>C
|
XP_006713135.1:p.Asp1400His
|
|
XM_011533533.2:c.4279G>C
|
XP_011531835.1:p.Asp1427His
|
|
XM_017006010.1:c.4279G>C
|
XP_016861499.1:p.Asp1427His
|
|
XM_017006011.1:c.4258G>C
|
XP_016861500.1:p.Asp1420His
|
|
XM_017006012.1:c.4198G>C
|
XP_016861501.1:p.Asp1400His
|
|
XM_017006013.1:c.4279G>C
|
XP_016861502.1:p.Asp1427His
|
|
XM_017006014.1:c.4177G>C
|
XP_016861503.1:p.Asp1393His
|
|
XM_017006015.1:c.3910G>C
|
XP_016861504.1:p.Asp1304His
|
|
XM_017006016.1:c.3739G>C
|
XP_016861505.1:p.Asp1247His
|
|
XM_017006017.1:c.751G>C
|
XP_016861506.1:p.Asp251His
|
|
XR_940397.2:n.4455G>C
|
|
|
NM_001365116.2:c.4177G>C
|
NP_001352045.1:p.Asp1393His
|
|
NM_015175.3:c.4279G>C
MANE Select
|
NP_055990.1:p.Asp1427His
|
|