ENST00000491889.6:c.*239G>T
|
ENSP00000419914.1:n.*239G>T
|
|
ENST00000645252.2:n.152+32338G>T
|
|
|
ENST00000682749.1:c.411G>T
|
ENSP00000507306.1:p.Arg137Ser
|
|
ENST00000682846.1:c.131+7132G>T
|
ENSP00000507527.1:n.131+7132G>T
|
|
ENST00000381971.8:c.876G>T
MANE Select
|
ENSP00000371398.3:p.Arg292Ser
|
|
ENST00000645252.1:n.152+32338G>T
|
|
|
ENST00000324333.14:c.411G>T
|
ENSP00000325494.10:p.Arg137Ser
|
|
ENST00000381971.7:c.876G>T
|
ENSP00000371398.3:p.Arg292Ser
|
|
ENST00000490709.1:n.696G>T
|
|
|
NM_001042413.1:c.876G>T
|
NP_001035878.1:p.Arg292Ser
|
|
NM_152629.3:c.411G>T
|
NP_689842.3:p.Arg137Ser
|
|
XM_005251386.3:c.411G>T
|
XP_005251443.1:p.Arg137Ser
|
|
XM_005251387.3:c.210G>T
|
XP_005251444.1:p.Arg70Ser
|
|
XM_005251388.3:c.210G>T
|
XP_005251445.1:p.Arg70Ser
|
|
XM_005251389.3:c.876G>T
|
XP_005251446.1:p.Arg292Ser
|
|
XM_006716731.2:c.876G>T
|
XP_006716794.1:p.Arg292Ser
|
|
XM_011517763.1:c.876G>T
|
XP_011516065.1:p.Arg292Ser
|
|
XM_011517764.1:c.876G>T
|
XP_011516066.1:p.Arg292Ser
|
|
XM_011517765.1:c.876G>T
|
XP_011516067.1:p.Arg292Ser
|
|
XM_011517766.1:c.411G>T
|
XP_011516068.1:p.Arg137Ser
|
|
XM_011517767.1:c.210G>T
|
XP_011516069.1:p.Arg70Ser
|
|
XM_011517768.1:c.876G>T
|
XP_011516070.1:p.Arg292Ser
|
|
XM_011517769.1:c.876G>T
|
XP_011516071.1:p.Arg292Ser
|
|
XR_929206.1:n.1642G>T
|
|
|
XM_005251386.4:c.411G>T
|
XP_005251443.1:p.Arg137Ser
|
|
XM_005251387.4:c.210G>T
|
XP_005251444.1:p.Arg70Ser
|
|
XM_005251388.4:c.210G>T
|
XP_005251445.1:p.Arg70Ser
|
|
XM_005251389.5:c.876G>T
|
XP_005251446.1:p.Arg292Ser
|
|
XM_006716731.3:c.876G>T
|
XP_006716794.1:p.Arg292Ser
|
|
XM_011517763.2:c.876G>T
|
XP_011516065.1:p.Arg292Ser
|
|
XM_011517764.2:c.876G>T
|
XP_011516066.1:p.Arg292Ser
|
|
XM_011517765.2:c.876G>T
|
XP_011516067.1:p.Arg292Ser
|
|
XM_011517766.2:c.411G>T
|
XP_011516068.1:p.Arg137Ser
|
|
XM_011517767.3:c.210G>T
|
XP_011516069.1:p.Arg70Ser
|
|
XM_011517769.2:c.876G>T
|
XP_011516071.1:p.Arg292Ser
|
|
XM_017014361.1:c.411G>T
|
XP_016869850.1:p.Arg137Ser
|
|
XR_929206.2:n.1638G>T
|
|
|
NM_001042413.2:c.876G>T
MANE Select
|
NP_001035878.1:p.Arg292Ser
|
|
NM_152629.4:c.411G>T
|
NP_689842.3:p.Arg137Ser
|
|