ENST00000529510.6:n.934T>C
|
|
|
ENST00000697845.1:n.858T>C
|
|
|
ENST00000697846.1:n.934T>C
|
|
|
ENST00000697847.1:n.934T>C
|
|
|
ENST00000697848.1:n.934T>C
|
|
|
ENST00000697849.1:n.1973T>C
|
|
|
ENST00000697850.1:n.934T>C
|
|
|
ENST00000697851.1:n.2294T>C
|
|
|
ENST00000638186.1:n.1008T>C
|
|
|
ENST00000638360.1:n.840T>C
|
|
|
ENST00000638925.1:n.941T>C
|
|
|
ENST00000650539.1:n.1110T>C
|
|
|
ENST00000330775.9:c.704T>C
|
ENSP00000476242.2:p.Val235Ala
|
|
ENST00000357590.9:c.704T>C
|
ENSP00000476176.2:p.Val235Ala
|
|
ENST00000524428.5:n.1026T>C
|
|
|
ENST00000525039.5:n.1128T>C
|
|
|
ENST00000525102.5:n.1462T>C
|
|
|
ENST00000525372.5:n.705T>C
|
|
|
ENST00000526275.5:n.1486T>C
|
|
|
ENST00000526626.6:n.667T>C
|
|
|
ENST00000527992.5:n.932T>C
|
|
|
ENST00000529510.5:n.478T>C
|
|
|
ENST00000530407.5:n.854T>C
|
|
|
ENST00000532085.1:n.3315T>C
|
|
|
ENST00000532888.6:n.1000T>C
|
|
|
ENST00000538950.5:c.485T>C
|
ENSP00000475991.2:p.Val162Ala
|
|
ENST00000545985.5:c.704T>C
|
ENSP00000475241.2:p.Val235Ala
|
|
NM_001164277.1:c.704T>C , LRG_187t1:c.704T>C
|
NP_001157749.1:p.Val235Ala
|
|
NM_001164278.1:c.704T>C
|
NP_001157750.1:p.Val235Ala
|
|
NM_001164279.1:c.485T>C
|
NP_001157751.1:p.Val162Ala
|
|
NM_001164280.1:c.704T>C
|
NP_001157752.1:p.Val235Ala
|
|
NM_001467.5:c.704T>C
|
NP_001458.1:p.Val235Ala
|
|
NM_001164278.2:c.704T>C
|
NP_001157750.1:p.Val235Ala
|
|
NM_001164279.2:c.485T>C
|
NP_001157751.1:p.Val162Ala
|
|
NM_001164280.2:c.704T>C
|
NP_001157752.1:p.Val235Ala
|
|
NM_001467.6:c.704T>C
|
NP_001458.1:p.Val235Ala
|
|
NM_001164277.2:c.704T>C
MANE Select
|
NP_001157749.1:p.Val235Ala
|
|