ENST00000233575.7:c.772G>C
MANE Select
|
ENSP00000233575.2:p.Glu258Gln
|
|
ENST00000233575.6:c.772G>C
|
ENSP00000233575.2:p.Glu258Gln
|
|
ENST00000427123.5:c.*582G>C
|
ENSP00000405399.1:n.*582G>C
|
|
ENST00000440760.5:c.*617G>C
|
ENSP00000399727.1:n.*617G>C
|
|
ENST00000453453.1:c.*299G>C
|
ENSP00000401922.1:n.*299G>C
|
|
ENST00000493711.1:n.489G>C
|
|
|
ENST00000494893.5:n.948G>C
|
|
|
ENST00000537606.5:c.697G>C
|
ENSP00000439208.1:p.Glu233Gln
|
|
NM_001267059.1:c.736G>C
|
NP_001253988.1:p.Glu246Gln
|
|
NM_001267060.1:c.697G>C
|
NP_001253989.1:p.Glu233Gln
|
|
NM_001267061.1:c.712G>C
|
NP_001253990.1:p.Glu238Gln
|
|
NM_014748.3:c.772G>C
|
NP_055563.1:p.Glu258Gln
|
|
NR_049782.1:n.1145G>C
|
|
|
NR_049783.1:n.1118G>C
|
|
|
NR_049784.1:n.1094G>C
|
|
|
NR_049785.1:n.1027G>C
|
|
|
NR_049786.1:n.976G>C
|
|
|
NR_049787.1:n.827G>C
|
|
|
NR_049788.1:n.757G>C
|
|
|
XM_011533203.1:c.130G>C
|
XP_011531505.1:p.Glu44Gln
|
|
XM_011533203.2:c.130G>C
|
XP_011531505.1:p.Glu44Gln
|
|
XM_017005405.2:c.130G>C
|
XP_016860894.1:p.Glu44Gln
|
|
NM_014748.4:c.772G>C
MANE Select
|
NP_055563.1:p.Glu258Gln
|
|
NM_001267059.2:c.736G>C
|
NP_001253988.1:p.Glu246Gln
|
|
NM_001267061.2:c.712G>C
|
NP_001253990.1:p.Glu238Gln
|
|
NR_049782.2:n.1025G>C
|
|
|
NR_049783.2:n.998G>C
|
|
|
NR_049784.2:n.974G>C
|
|
|
NR_049785.2:n.907G>C
|
|
|
NR_049786.2:n.856G>C
|
|
|
NR_049787.2:n.707G>C
|
|
|
NR_049788.2:n.637G>C
|
|
|
NM_001267060.2:c.697G>C
|
NP_001253989.1:p.Glu233Gln
|
|