ENST00000682153.1:c.7431A>T
|
ENSP00000507923.1:p.Pro2477=
|
|
ENST00000682358.1:n.7501A>T
|
|
|
ENST00000683334.1:c.*3113A>T
|
ENSP00000507369.1:n.*3113A>T
|
|
ENST00000357162.7:c.7356A>T
MANE Select
|
ENSP00000349685.2:p.Pro2452=
|
|
ENST00000358544.7:c.7431A>T
MANE Plus Clinical
|
ENSP00000351346.2:p.Pro2477=
|
|
ENST00000357162.6:c.7356A>T
|
ENSP00000349685.2:p.Pro2452=
|
|
ENST00000358544.6:c.7431A>T
|
ENSP00000351346.2:p.Pro2477=
|
|
ENST00000518569.1:n.378-1799A>T
|
|
|
NM_017890.4:c.7431A>T , LRG_351t1:c.7431A>T
|
NP_060360.3:p.Pro2477=
|
|
NM_152564.4:c.7356A>T , LRG_351t2:c.7356A>T
|
NP_689777.3:p.Pro2452=
|
|
XM_005250800.2:c.7431A>T
|
XP_005250857.1:p.Pro2477=
|
|
XM_005250801.3:c.7431A>T
|
XP_005250858.1:p.Pro2477=
|
|
XM_011516848.1:c.7428A>T
|
XP_011515150.1:p.Pro2476=
|
|
XM_011516849.1:c.7353A>T
|
XP_011515151.1:p.Pro2451=
|
|
XM_011516850.1:c.7053A>T
|
XP_011515152.1:p.Pro2351=
|
|
XM_011516851.1:c.4317A>T
|
XP_011515153.1:p.Pro1439=
|
|
XM_011516852.1:c.4317A>T
|
XP_011515154.1:p.Pro1439=
|
|
XM_011516853.1:c.7431A>T
|
XP_011515155.1:p.Pro2477=
|
|
XM_011516854.1:c.3210A>T
|
XP_011515156.1:p.Pro1070=
|
|
XR_928446.1:n.1830+5595T>A
|
|
|
XM_005250800.3:c.7431A>T
|
XP_005250857.1:p.Pro2477=
|
|
XM_005250801.5:c.7431A>T
|
XP_005250858.1:p.Pro2477=
|
|
XM_011516848.2:c.7428A>T
|
XP_011515150.1:p.Pro2476=
|
|
XM_011516849.2:c.7353A>T
|
XP_011515151.1:p.Pro2451=
|
|
XM_011516850.2:c.7053A>T
|
XP_011515152.1:p.Pro2351=
|
|
XM_011516851.2:c.4317A>T
|
XP_011515153.1:p.Pro1439=
|
|
XM_011516852.2:c.4317A>T
|
XP_011515154.1:p.Pro1439=
|
|
XM_011516853.2:c.7431A>T
|
XP_011515155.1:p.Pro2477=
|
|
XM_011516854.2:c.3210A>T
|
XP_011515156.1:p.Pro1070=
|
|
XM_017013109.1:c.7236A>T
|
XP_016868598.1:p.Pro2412=
|
|
XM_017013111.1:c.4317A>T
|
XP_016868600.1:p.Pro1439=
|
|
XM_017013112.1:c.2988A>T
|
XP_016868601.1:p.Pro996=
|
|
XM_024447074.1:c.6216A>T
|
XP_024302842.1:p.Pro2072=
|
|
NM_017890.5:c.7431A>T
MANE Plus Clinical
|
NP_060360.3:p.Pro2477=
|
|
NM_152564.5:c.7356A>T
MANE Select
|
NP_689777.3:p.Pro2452=
|
|