NM_001004697.2:c.199A>G
(OR2T5)
MANE Select
|
NP_001004697.1:p.Ile67Val
|
ENST00000641363.1:c.199A>G
(OR2T5)
MANE Select
|
ENSP00000493066.1:p.Ile67Val
|
NM_001004697.1:c.199A>G
(OR2T5)
|
NP_001004697.1:p.Ile67Val
|
ENST00000366473.3:c.199A>G
(OR2T5)
|
ENSP00000355429.2:p.Ile67Val
|
XR_001738575.1:n.144-3303T>C
|
|
XR_002958498.1:n.1101-3303T>C
|
|
XR_949139.1:n.77+39395A>G
(OR2T2)
|
|
XR_949140.1:n.137-3303T>C
(OR14I1)
|
|
XR_949141.1:n.1089-3303T>C
(OR14I1)
|
|
XR_949142.1:n.144-3303T>C
(OR14I1)
|
|
XR_949143.1:n.137-3303T>C
(OR14I1)
|
|
XR_949371.1:n.63+43118A>G
|
|