|
ENST00000517417.3:c.2421+31536T>C
(PCDHGA1)
MANE Select
|
ENSP00000431083.1:n.2421+31536T>C
|
|
|
ENST00000518069.2:c.311T>C
(PCDHGA5)
MANE Select
|
ENSP00000429834.1:p.Val104Ala
|
|
|
ENST00000522605.2:c.2421+2085T>C
(PCDHGB2)
MANE Select
|
ENSP00000429018.1:n.2421+2085T>C
|
|
|
ENST00000523390.2:c.2409+11972T>C
(PCDHGB1)
MANE Select
|
ENSP00000429273.1:n.2409+11972T>C
|
|
|
ENST00000253812.8:c.2424+18184T>C
(PCDHGA3)
MANE Select
|
ENSP00000253812.7:n.2424+18184T>C
|
|
|
ENST00000394576.3:c.2424+23246T>C
(PCDHGA2)
MANE Select
|
ENSP00000378077.2:n.2424+23246T>C
|
|
|
ENST00000571252.3:c.2514+7020T>C
(PCDHGA4)
MANE Select
|
ENSP00000458570.2:n.2514+7020T>C
|
|
|
ENST00000253812.7:c.2424+18184T>C
(PCDHGA3)
|
ENSP00000253812.6:n.2424+18184T>C
|
|
|
ENST00000394576.2:c.2424+23246T>C
(PCDHGA2)
|
ENSP00000378077.2:n.2424+23246T>C
|
|
|
ENST00000517417.2:c.2421+31536T>C
(PCDHGA1)
|
ENSP00000431083.1:n.2421+31536T>C
|
|
|
ENST00000518069.1:c.311T>C
(PCDHGA5)
|
ENSP00000429834.1:p.Val104Ala
|
|
|
ENST00000522605.1:c.2421+2085T>C
(PCDHGB2)
|
ENSP00000429018.1:n.2421+2085T>C
|
|
|
ENST00000523390.1:c.2409+11972T>C
(PCDHGB1)
|
ENSP00000429273.1:n.2409+11972T>C
|
|
|
ENST00000571252.2:c.2514+7020T>C
(PCDHGA4)
|
ENSP00000458570.2:n.2514+7020T>C
|
|
|
ENST00000611914.1:c.311T>C
(PCDHGA5)
|
ENSP00000480337.1:p.Val104Ala
|
|
|
ENST00000612467.1:c.2327+18184T>C
(PCDHGA3)
|
ENSP00000481801.1:n.2327+18184T>C
|
|
|
NM_018912.2:c.2421+31536T>C
(PCDHGA1)
|
NP_061735.1:n.2421+31536T>C
|
|
|
NM_018915.3:c.2424+23246T>C
(PCDHGA2)
|
NP_061738.1:n.2424+23246T>C
|
|
|
NM_018916.3:c.2424+18184T>C
(PCDHGA3)
|
NP_061739.2:n.2424+18184T>C
|
|
|
NM_018917.3:c.2514+7020T>C
(PCDHGA4)
|
NP_061740.2:n.2514+7020T>C
|
|
|
NM_018918.2:c.311T>C
(PCDHGA5)
|
NP_061741.1:p.Val104Ala
|
|
|
NM_018922.2:c.2409+11972T>C
(PCDHGB1)
|
NP_061745.1:n.2409+11972T>C
|
|
|
NM_018923.2:c.2421+2085T>C
(PCDHGB2)
|
NP_061746.1:n.2421+2085T>C
|
|
|
NM_032054.1:c.311T>C
(PCDHGA5)
|
NP_114443.1:p.Val104Ala
|
|
|
NM_018915.4:c.2424+23246T>C
(PCDHGA2)
MANE Select
|
NP_061738.1:n.2424+23246T>C
|
|
|
NM_018917.4:c.2514+7020T>C
(PCDHGA4)
MANE Select
|
NP_061740.2:n.2514+7020T>C
|
|
|
NM_018916.4:c.2424+18184T>C
(PCDHGA3)
MANE Select
|
NP_061739.2:n.2424+18184T>C
|
|
|
NM_018912.3:c.2421+31536T>C
(PCDHGA1)
MANE Select
|
NP_061735.1:n.2421+31536T>C
|
|
|
NM_018918.3:c.311T>C
(PCDHGA5)
MANE Select
|
NP_061741.1:p.Val104Ala
|
|
|
NM_018922.3:c.2409+11972T>C
(PCDHGB1)
MANE Select
|
NP_061745.1:n.2409+11972T>C
|
|
|
NM_018923.3:c.2421+2085T>C
(PCDHGB2)
MANE Select
|
NP_061746.1:n.2421+2085T>C
|
|
|
NM_032054.2:c.311T>C
(PCDHGA5)
|
NP_114443.1:p.Val104Ala
|
|
