ENST00000354393.7:c.1057T>G
|
ENSP00000346369.2:p.Phe353Val
|
|
ENST00000373675.4:c.1882T>G
|
ENSP00000362779.4:p.Phe628Val
|
|
ENST00000540630.6:c.1936T>G
|
ENSP00000441668.3:p.Phe646Val
|
|
ENST00000613327.5:c.1882T>G
|
ENSP00000480757.2:p.Phe628Val
|
|
ENST00000687572.1:c.760T>G
|
ENSP00000510427.1:p.Phe254Val
|
|
ENST00000688812.1:c.1858T>G
|
ENSP00000510658.1:p.Phe620Val
|
|
ENST00000690544.1:c.*1153T>G
|
ENSP00000508989.1:n.*1153T>G
|
|
ENST00000358913.10:c.1882T>G
MANE Select
|
ENSP00000351790.5:p.Phe628Val
|
|
ENST00000354393.6:c.1057T>G
|
ENSP00000346369.2:p.Phe353Val
|
|
ENST00000358913.9:c.1882T>G
|
ENSP00000351790.5:p.Phe628Val
|
|
ENST00000540630.5:c.1882T>G
|
ENSP00000441668.2:p.Phe628Val
|
|
ENST00000613327.4:c.1000T>G
|
ENSP00000480757.1:p.Phe334Val
|
|
NM_001256267.1:c.1882T>G
|
NP_001243196.1:p.Phe628Val
|
|
NM_001256268.1:c.1000T>G
|
NP_001243197.1:p.Phe334Val
|
|
NM_032578.3:c.1882T>G , LRG_410t1:c.1882T>G
|
NP_115967.2:p.Phe628Val
|
|
NR_045662.3:n.1309T>G
|
|
|
NR_045663.3:n.2150T>G
|
|
|
XM_006718043.2:c.1936T>G
|
XP_006718106.1:p.Phe646Val
|
|
XM_011540292.1:c.1912T>G
|
XP_011538594.1:p.Phe638Val
|
|
XM_017016833.1:c.1960T>G
|
XP_016872322.1:p.Phe654Val
|
|
XM_017016834.2:c.1882T>G
|
XP_016872323.1:p.Phe628Val
|
|
XM_024448236.1:c.760T>G
|
XP_024304004.1:p.Phe254Val
|
|
NR_045662.4:n.1419T>G
|
|
|
NR_045663.4:n.2095T>G
|
|
|
NM_001256267.2:c.1882T>G
|
NP_001243196.1:p.Phe628Val
|
|
NM_001256268.2:c.1000T>G
|
NP_001243197.1:p.Phe334Val
|
|
NM_032578.4:c.1882T>G
MANE Select
|
NP_115967.2:p.Phe628Val
|
|