ENST00000545279.6:c.*887A>G
MANE Select
|
ENSP00000441954.2:n.*887A>G
|
|
ENST00000513418.1:c.164+3735A>G
|
|
|
ENST00000545279.5:c.*887A>G
|
ENSP00000441954.2:n.*887A>G
|
|
ENST00000545620.5:c.*887A>G
|
ENSP00000446474.2:n.*887A>G
|
|
NM_001001419.2:c.*887A>G
|
NP_001001419.1:n.*887A>G
|
|
NM_001001420.2:c.*887A>G
|
NP_001001420.1:n.*887A>G
|
|
NM_005903.6:c.*887A>G
|
NP_005894.3:n.*887A>G
|
|
XM_017009470.2:c.*887A>G
|
XP_016864959.1:n.*887A>G
|
|
XM_024446046.1:c.*887A>G
|
XP_024301814.1:n.*887A>G
|
|
XM_024446047.1:c.*887A>G
|
XP_024301815.1:n.*887A>G
|
|
NM_005903.7:c.*887A>G
MANE Select
|
NP_005894.3:n.*887A>G
|
|
NM_001001419.3:c.*887A>G
|
NP_001001419.1:n.*887A>G
|
|
NM_001001420.3:c.*887A>G
|
NP_001001420.1:n.*887A>G
|
|