ENST00000490576.2:c.*2371T>C
(CYP1B1)
|
ENSP00000478839.2:n.*2371T>C
|
|
ENST00000610745.5:c.*2371T>C
(CYP1B1)
MANE Select
|
ENSP00000478561.1:n.*2371T>C
|
|
ENST00000491456.1:n.184+827T>C
(CYP1B1)
|
|
|
ENST00000610745.4:c.*2371T>C
(CYP1B1)
|
ENSP00000478561.1:n.*2371T>C
|
|
NM_000104.3:c.*2371T>C
(CYP1B1)
|
NP_000095.2:n.*2371T>C
|
|
XR_939668.1:n.3351A>G
(RMDN2)
|
|
|
XM_011532615.3:c.*1397A>G
(RMDN2)
|
XP_011530917.2:n.*1397A>G
|
|
XM_017003475.2:c.*1361A>G
(RMDN2)
|
XP_016858964.1:n.*1361A>G
|
|
XR_939668.3:n.3482A>G
(RMDN2)
|
|
|
NM_000104.4:c.*2371T>C
(CYP1B1)
MANE Select
|
NP_000095.2:n.*2371T>C
|
|