ENST00000423778.7:c.50T>C
(KY)
MANE Select
|
ENSP00000397598.2:p.Ile17Thr
|
|
ENST00000423778.6:c.50T>C
(KY)
|
ENSP00000397598.2:p.Ile17Thr
|
|
ENST00000460895.5:c.-153+35473A>G
(EPHB1)
|
ENSP00000417435.1:n.-153+35473A>G
|
|
ENST00000467708.2:n.361+35473A>G
(EPHB1)
|
|
|
ENST00000503669.1:c.50T>C
(KY)
|
ENSP00000426777.1:p.Ile17Thr
|
|
ENST00000506319.5:n.726T>C
(KY)
|
|
|
ENST00000508956.5:c.50T>C
(KY)
|
ENSP00000421297.1:p.Ile17Thr
|
|
NM_178554.4:c.50T>C
(KY)
|
NP_848649.3:p.Ile17Thr
|
|
XM_005247417.2:c.227T>C
(KY)
|
XP_005247474.1:p.Ile76Thr
|
|
XM_005247418.2:c.227T>C
(KY)
|
XP_005247475.1:p.Ile76Thr
|
|
XM_006713612.2:c.227T>C
(KY)
|
XP_006713675.1:p.Ile76Thr
|
|
XR_241572.2:n.540-7773A>G
|
|
|
XR_924521.1:n.540-22043A>G
|
|
|
NM_001350859.1:c.50T>C
(KY)
|
NP_001337788.1:p.Ile17Thr
|
|
NM_001350860.1:c.50T>C
(KY)
|
NP_001337789.1:p.Ile17Thr
|
|
NM_001366276.1:c.50T>C
(KY)
|
NP_001353205.1:p.Ile17Thr
|
|
NM_001366277.1:c.50T>C
(KY)
|
NP_001353206.1:p.Ile17Thr
|
|
NM_178554.5:c.50T>C
(KY)
|
NP_848649.3:p.Ile17Thr
|
|
XM_006713612.3:c.227T>C
(KY)
|
XP_006713675.1:p.Ile76Thr
|
|
XM_017006287.1:c.227T>C
(KY)
|
XP_016861776.1:p.Ile76Thr
|
|
XM_017006288.1:c.227T>C
(KY)
|
XP_016861777.1:p.Ile76Thr
|
|
XM_017006290.1:c.227T>C
(KY)
|
XP_016861779.1:p.Ile76Thr
|
|
XM_024453389.1:c.-153+35473A>G
(EPHB1)
|
XP_024309157.1:n.-153+35473A>G
|
|
XM_024453390.1:c.-153+35473A>G
(EPHB1)
|
XP_024309158.1:n.-153+35473A>G
|
|
XM_024453508.1:c.227T>C
(KY)
|
XP_024309276.1:p.Ile76Thr
|
|
XR_002959586.1:n.1927+35473A>G
(CEP63)
|
|
|
NM_178554.6:c.50T>C
(KY)
MANE Select
|
NP_848649.3:p.Ile17Thr
|
|
NM_001350859.2:c.50T>C
(KY)
|
NP_001337788.1:p.Ile17Thr
|
|
NM_001350860.2:c.50T>C
(KY)
|
NP_001337789.1:p.Ile17Thr
|
|
NM_001366277.2:c.50T>C
(KY)
|
NP_001353206.1:p.Ile17Thr
|
|