ENST00000366159.9:n.441G>C
|
|
|
ENST00000437813.8:c.407G>C
|
ENSP00000513672.1:p.Trp136Ser
|
|
ENST00000440083.7:c.407G>C
|
ENSP00000413224.3:p.Trp136Ser
|
|
ENST00000535958.2:c.*234G>C
|
ENSP00000513673.1:n.*234G>C
|
|
ENST00000698339.1:c.407G>C
|
ENSP00000513670.1:p.Trp136Ser
|
|
ENST00000698340.1:c.407G>C
|
ENSP00000513671.1:p.Trp136Ser
|
|
ENST00000162749.7:c.407G>C
MANE Select
|
ENSP00000162749.2:p.Trp136Ser
|
|
ENST00000162749.6:c.407G>C
|
ENSP00000162749.2:p.Trp136Ser
|
|
ENST00000366159.8:c.407G>C
|
ENSP00000380389.3:p.Trp136Ser
|
|
ENST00000437813.7:n.368G>C
|
|
|
ENST00000440083.6:c.407G>C
|
ENSP00000413224.2:p.Trp136Ser
|
|
ENST00000534885.5:c.253G>C
|
ENSP00000441803.1:p.Gly85Arg
|
|
ENST00000537842.5:n.11G>C
|
|
|
ENST00000539372.5:c.407G>C
|
ENSP00000442059.1:p.Trp136Ser
|
|
ENST00000540022.5:c.278G>C
|
ENSP00000438343.1:p.Trp93Ser
|
|
ENST00000543048.5:c.*18G>C
|
ENSP00000439981.1:n.*18G>C
|
|
ENST00000543995.5:c.213G>C
|
ENSP00000442405.1:p.Leu71Phe
|
|
NM_001065.3:c.407G>C , LRG_193t1:c.407G>C
|
NP_001056.1:p.Trp136Ser
|
|
NM_001346091.1:c.83G>C
|
NP_001333020.1:p.Trp28Ser
|
|
NM_001346092.1:c.-171G>C
|
NP_001333021.1:n.-171G>C
|
|
NR_144351.1:n.710G>C
|
|
|
NM_001065.4:c.407G>C
MANE Select
|
NP_001056.1:p.Trp136Ser
|
|
NM_001346091.2:c.83G>C
|
NP_001333020.1:p.Trp28Ser
|
|
NM_001346092.2:c.-171G>C
|
NP_001333021.1:n.-171G>C
|
|
NR_144351.2:n.669G>C
|
|
|