ENST00000366159.9:n.464T>G
|
|
|
ENST00000437813.8:c.430T>G
|
ENSP00000513672.1:p.Phe144Val
|
|
ENST00000440083.7:c.430T>G
|
ENSP00000413224.3:p.Phe144Val
|
|
ENST00000535958.2:c.*257T>G
|
ENSP00000513673.1:n.*257T>G
|
|
ENST00000698339.1:c.430T>G
|
ENSP00000513670.1:p.Phe144Val
|
|
ENST00000698340.1:c.430T>G
|
ENSP00000513671.1:p.Phe144Val
|
|
ENST00000162749.7:c.430T>G
MANE Select
|
ENSP00000162749.2:p.Phe144Val
|
|
ENST00000162749.6:c.430T>G
|
ENSP00000162749.2:p.Phe144Val
|
|
ENST00000366159.8:c.430T>G
|
ENSP00000380389.3:p.Phe144Val
|
|
ENST00000437813.7:n.391T>G
|
|
|
ENST00000440083.6:c.430T>G
|
ENSP00000413224.2:p.Phe144Val
|
|
ENST00000534885.5:c.276T>G
|
ENSP00000441803.1:p.Ala92=
|
|
ENST00000537842.5:n.34T>G
|
|
|
ENST00000539372.5:c.430T>G
|
ENSP00000442059.1:p.Phe144Val
|
|
ENST00000540022.5:c.301T>G
|
ENSP00000438343.1:p.Phe101Val
|
|
ENST00000543048.5:c.*41T>G
|
ENSP00000439981.1:n.*41T>G
|
|
ENST00000543995.5:c.*17T>G
|
ENSP00000442405.1:n.*17T>G
|
|
NM_001065.3:c.430T>G , LRG_193t1:c.430T>G
|
NP_001056.1:p.Phe144Val
|
|
NM_001346091.1:c.106T>G
|
NP_001333020.1:p.Phe36Val
|
|
NM_001346092.1:c.-148T>G
|
NP_001333021.1:n.-148T>G
|
|
NR_144351.1:n.733T>G
|
|
|
NM_001065.4:c.430T>G
MANE Select
|
NP_001056.1:p.Phe144Val
|
|
NM_001346091.2:c.106T>G
|
NP_001333020.1:p.Phe36Val
|
|
NM_001346092.2:c.-148T>G
|
NP_001333021.1:n.-148T>G
|
|
NR_144351.2:n.692T>G
|
|
|