ENST00000698234.1:n.1548G>A
|
|
|
ENST00000698317.1:n.2164G>A
|
|
|
ENST00000698318.1:n.1947G>A
|
|
|
ENST00000698319.1:n.1310G>A
|
|
|
ENST00000698320.1:n.1198G>A
|
|
|
ENST00000470127.2:n.1211G>A
|
|
|
ENST00000475699.6:c.702G>A
|
ENSP00000419854.3:p.Leu234=
|
|
ENST00000483674.3:n.620G>A
|
|
|
ENST00000601016.6:c.738G>A
MANE Select
|
ENSP00000469981.1:p.Leu246=
|
|
ENST00000612012.5:c.696G>A
|
ENSP00000482070.2:p.Leu232=
|
|
ENST00000612460.5:c.648G>A
|
ENSP00000481037.1:p.Leu216=
|
|
ENST00000614595.2:n.2085G>A
|
|
|
ENST00000615658.5:n.1327G>A
|
|
|
ENST00000616020.5:c.750G>A
|
ENSP00000483636.2:p.Leu250=
|
|
ENST00000617701.5:c.*751G>A
|
ENSP00000481645.1:n.*751G>A
|
|
ENST00000651139.1:c.-46G>A
|
ENSP00000498957.1:n.-46G>A
|
|
ENST00000652354.1:c.420G>A
|
ENSP00000498734.1:p.Leu140=
|
|
ENST00000652358.1:c.531G>A
|
ENSP00000498464.1:p.Leu177=
|
|
ENST00000652390.1:c.657G>A
|
ENSP00000498858.1:p.Leu219=
|
|
ENST00000652476.1:n.1404G>A
|
|
|
ENST00000652644.1:c.351G>A
|
ENSP00000498496.1:p.Leu117=
|
|
ENST00000652682.1:c.795G>A
|
ENSP00000498288.1:p.Leu265=
|
|
ENST00000652685.1:n.1091G>A
|
|
|
ENST00000369776.8:c.648G>A
|
ENSP00000358791.4:p.Leu216=
|
|
ENST00000426231.5:c.735G>A
|
|
|
ENST00000475699.5:c.696G>A
|
ENSP00000419854.2:p.Leu232=
|
|
ENST00000494912.5:n.1427G>A
|
|
|
ENST00000498029.1:n.196G>A
|
|
|
ENST00000601016.5:c.738G>A
|
ENSP00000469981.1:p.Leu246=
|
|
ENST00000612460.4:c.648G>A
|
ENSP00000481037.1:p.Leu216=
|
|
ENST00000613002.4:c.606G>A
|
ENSP00000478154.1:p.Leu202=
|
|
ENST00000615986.4:c.*466G>A
|
ENSP00000480133.1:n.*466G>A
|
|
NM_000116.4:c.738G>A
|
NP_000107.1:p.Leu246=
|
|
NM_001303465.1:c.750G>A
|
NP_001290394.1:p.Leu250=
|
|
NM_181311.3:c.648G>A
|
NP_851828.1:p.Leu216=
|
|
NM_181312.3:c.696G>A
|
NP_851829.1:p.Leu232=
|
|
NM_181313.3:c.606G>A
|
NP_851830.1:p.Leu202=
|
|
NR_024048.2:n.1080G>A
|
|
|
XM_006724836.1:c.792G>A
|
XP_006724899.1:p.Leu264=
|
|
XM_006724837.1:c.777G>A
|
XP_006724900.1:p.Leu259=
|
|
XM_006724839.1:c.660G>A
|
XP_006724902.1:p.Leu220=
|
|
XM_006724841.2:c.531G>A
|
XP_006724904.1:p.Leu177=
|
|
XM_006724842.2:c.441G>A
|
XP_006724905.1:p.Leu147=
|
|
XM_011531189.1:c.579G>A
|
XP_011529491.1:p.Leu193=
|
|
XM_011531190.1:c.531G>A
|
XP_011529492.1:p.Leu177=
|
|
XM_011531191.1:c.462G>A
|
XP_011529493.1:p.Leu154=
|
|
XM_011531192.1:c.459G>A
|
XP_011529494.1:p.Leu153=
|
|
XR_938511.1:n.1086G>A
|
|
|
XM_006724841.4:c.531G>A
|
XP_006724904.1:p.Leu177=
|
|
XM_006724842.4:c.441G>A
|
XP_006724905.1:p.Leu147=
|
|
XM_011531191.2:c.462G>A
|
XP_011529493.1:p.Leu154=
|
|
XM_017029761.1:c.723G>A
|
XP_016885250.1:p.Leu241=
|
|
XM_017029762.1:c.702G>A
|
XP_016885251.1:p.Leu234=
|
|
XM_017029763.1:c.525G>A
|
XP_016885252.1:p.Leu175=
|
|
XM_017029764.1:c.459G>A
|
XP_016885253.1:p.Leu153=
|
|
XM_017029765.2:c.399G>A
|
XP_016885254.1:p.Leu133=
|
|
XM_024452431.1:c.696G>A
|
XP_024308199.1:p.Leu232=
|
|
NM_000116.5:c.738G>A
MANE Select
|
NP_000107.1:p.Leu246=
|
|
NM_001303465.2:c.750G>A
|
NP_001290394.1:p.Leu250=
|
|
NM_181311.4:c.648G>A
|
NP_851828.1:p.Leu216=
|
|
NM_181312.4:c.696G>A
|
NP_851829.1:p.Leu232=
|
|
NM_181313.4:c.606G>A
|
NP_851830.1:p.Leu202=
|
|
NR_024048.3:n.1059G>A
|
|
|