ENST00000395184.6:c.181-1889A>T
MANE Select
|
ENSP00000378611.1:n.181-1889A>T
|
|
ENST00000395184.5:c.181-1889A>T
|
ENSP00000378611.1:n.181-1889A>T
|
|
ENST00000503995.5:c.181-1889A>T
|
ENSP00000423206.1:n.181-1889A>T
|
|
ENST00000506421.5:n.318-1889A>T
|
|
|
ENST00000509709.1:n.130-1889A>T
|
|
|
ENST00000512201.5:c.-105-1889A>T
|
ENSP00000426105.1:n.-105-1889A>T
|
|
NM_001025616.2:c.181-1889A>T
|
NP_001020787.2:n.181-1889A>T
|
|
XM_005263263.3:c.181-1889A>T
|
XP_005263320.1:n.181-1889A>T
|
|
XM_024454238.1:c.-105-1889A>T
|
XP_024310006.1:n.-105-1889A>T
|
|
XM_024454239.1:c.-105-1889A>T
|
XP_024310007.1:n.-105-1889A>T
|
|
NM_001025616.3:c.181-1889A>T
MANE Select
|
NP_001020787.2:n.181-1889A>T
|
|