ENST00000347401.8:c.281C>T
|
|
|
ENST00000353578.9:c.7018C>T
|
ENSP00000315873.4:p.Gln2340Ter
|
|
ENST00000295550.9:c.7636C>T
MANE Select
|
ENSP00000295550.4:p.Gln2546Ter
|
|
ENST00000295550.8:c.7636C>T
|
ENSP00000295550.4:p.Gln2546Ter
|
|
ENST00000347401.7:c.5812C>T
|
ENSP00000315609.4:p.Gln1938Ter
|
|
ENST00000353578.8:c.7018C>T
|
ENSP00000315873.4:p.Gln2340Ter
|
|
ENST00000409809.5:c.7018C>T
|
ENSP00000386844.1:p.Gln2340Ter
|
|
ENST00000472056.5:c.5815C>T
|
ENSP00000418285.1:p.Gln1939Ter
|
|
ENST00000491769.1:n.1890C>T
|
|
|
NM_004369.3:c.7636C>T , LRG_473t1:c.7636C>T
|
NP_004360.2:p.Gln2546Ter
|
|
NM_057166.4:c.5815C>T
|
NP_476507.3:p.Gln1939Ter
|
|
NM_057167.3:c.7018C>T
|
NP_476508.2:p.Gln2340Ter
|
|
XM_005246065.1:c.7036C>T
|
XP_005246122.1:p.Gln2346Ter
|
|
XM_005246066.1:c.6415C>T
|
XP_005246123.1:p.Gln2139Ter
|
|
XM_006712253.1:c.7135C>T
|
XP_006712316.1:p.Gln2379Ter
|
|
XM_011510574.1:c.7633C>T
|
XP_011508876.1:p.Gln2545Ter
|
|
XM_011510575.1:c.5230C>T
|
XP_011508877.1:p.Gln1744Ter
|
|
XM_017003304.1:c.5230C>T
|
XP_016858793.1:p.Gln1744Ter
|
|
XM_024452684.1:c.6415C>T
|
XP_024308452.1:p.Gln2139Ter
|
|
NM_004369.4:c.7636C>T
MANE Select
|
NP_004360.2:p.Gln2546Ter
|
|
NM_057166.5:c.5815C>T
|
NP_476507.3:p.Gln1939Ter
|
|
NM_057167.4:c.7018C>T
|
NP_476508.2:p.Gln2340Ter
|
|