ENST00000270301.12:c.4236G>T
|
ENSP00000270301.6:p.Val1412=
|
|
ENST00000401500.7:c.4251G>T
MANE Select
|
ENSP00000384792.1:p.Val1417=
|
|
ENST00000587391.6:c.*4111G>T
|
ENSP00000465525.1:n.*4111G>T
|
|
ENST00000679357.1:c.2331G>T
|
|
|
ENST00000679598.1:c.996G>T
|
|
|
ENST00000679682.1:c.4236G>T
|
ENSP00000506226.1:p.Val1412=
|
|
ENST00000679714.1:c.4245G>T
|
ENSP00000506627.1:p.Val1415=
|
|
ENST00000679757.1:c.3900G>T
|
ENSP00000505158.1:p.Val1300=
|
|
ENST00000679858.1:c.*3633G>T
|
ENSP00000505655.1:n.*3633G>T
|
|
ENST00000680211.1:c.852G>T
|
ENSP00000506102.1:p.Val284=
|
|
ENST00000680280.1:n.1754G>T
|
|
|
ENST00000680349.1:n.2900G>T
|
|
|
ENST00000680403.1:c.4236G>T
|
ENSP00000505677.1:p.Val1412=
|
|
ENST00000680564.1:c.4002G>T
|
ENSP00000505582.1:p.Val1334=
|
|
ENST00000680590.1:c.*2631G>T
|
ENSP00000505350.1:n.*2631G>T
|
|
ENST00000680597.1:c.984G>T
|
|
|
ENST00000680739.1:c.1266G>T
|
|
|
ENST00000680773.1:n.2752G>T
|
|
|
ENST00000680806.1:c.*3554G>T
|
ENSP00000506418.1:n.*3554G>T
|
|
ENST00000680997.1:n.2183G>T
|
|
|
ENST00000681608.1:n.2096G>T
|
|
|
ENST00000681625.1:c.*1583G>T
|
ENSP00000505555.1:n.*1583G>T
|
|
ENST00000681648.1:n.2302G>T
|
|
|
ENST00000270301.11:c.4236G>T
|
ENSP00000270301.6:p.Val1412=
|
|
ENST00000401500.6:c.4251G>T
|
ENSP00000384792.1:p.Val1417=
|
|
ENST00000587391.5:c.*4111G>T
|
ENSP00000465525.1:n.*4111G>T
|
|
NM_001083961.1:c.4251G>T
|
NP_001077430.1:p.Val1417=
|
|
NM_173636.4:c.4236G>T
|
NP_775907.4:p.Val1412=
|
|
XM_005258809.2:c.4140G>T
|
XP_005258866.1:p.Val1380=
|
|
XM_011526837.1:c.4236G>T
|
XP_011525139.1:p.Val1412=
|
|
XM_011526838.1:c.4002G>T
|
XP_011525140.1:p.Val1334=
|
|
XM_011526839.1:c.3900G>T
|
XP_011525141.1:p.Val1300=
|
|
XM_011526840.1:c.3243G>T
|
XP_011525142.1:p.Val1081=
|
|
XM_011526841.1:c.2829G>T
|
XP_011525143.1:p.Val943=
|
|
XM_011526842.1:c.2682G>T
|
XP_011525144.1:p.Val894=
|
|
XM_011526843.1:c.1998G>T
|
XP_011525145.1:p.Val666=
|
|
XM_011526844.1:c.1998G>T
|
XP_011525146.1:p.Val666=
|
|
XM_011526840.2:c.3243G>T
|
XP_011525142.1:p.Val1081=
|
|
XM_011526841.2:c.2829G>T
|
XP_011525143.1:p.Val943=
|
|
XM_011526844.2:c.1998G>T
|
XP_011525146.1:p.Val666=
|
|
XM_017026665.1:c.4251G>T
|
XP_016882154.1:p.Val1417=
|
|
NM_001083961.2:c.4251G>T
MANE Select
|
NP_001077430.1:p.Val1417=
|
|
NM_173636.5:c.4236G>T
|
NP_775907.4:p.Val1412=
|
|