ENST00000225573.5:c.*236A>G
|
ENSP00000225573.5:n.*236A>G
|
|
ENST00000434554.7:c.*236A>G
|
ENSP00000399960.3:n.*236A>G
|
|
ENST00000582171.6:c.*687A>G
|
ENSP00000463994.1:n.*687A>G
|
|
ENST00000584806.2:n.691A>G
|
|
|
ENST00000641305.1:n.2521A>G
|
|
|
ENST00000641323.1:c.*1041A>G
|
ENSP00000492965.1:n.*1041A>G
|
|
ENST00000641427.1:n.1022A>G
|
|
|
ENST00000641703.1:c.738A>G
|
ENSP00000493219.1:n.738A>G
|
|
ENST00000641709.1:c.*844A>G
|
ENSP00000493349.1:n.*844A>G
|
|
ENST00000641856.1:c.*1530A>G
|
ENSP00000493224.1:n.*1530A>G
|
|
ENST00000642017.2:c.*236A>G
MANE Select
|
ENSP00000493302.2:n.*236A>G
|
|
ENST00000225573.4:c.*236A>G
|
ENSP00000225573.4:n.*236A>G
|
|
ENST00000434554.6:c.*236A>G
|
ENSP00000399960.2:n.*236A>G
|
|
ENST00000582171.5:c.*687A>G
|
ENSP00000463994.1:n.*687A>G
|
|
NM_018129.3:c.*236A>G
|
NP_060599.1:n.*236A>G
|
|
XM_005257500.2:c.*236A>G
|
XP_005257557.1:n.*236A>G
|
|
XM_011524968.1:c.*236A>G
|
XP_011523270.1:n.*236A>G
|
|
XM_005257500.3:c.*236A>G
|
XP_005257557.1:n.*236A>G
|
|
XM_011524968.2:c.*236A>G
|
XP_011523270.1:n.*236A>G
|
|
XM_017024813.1:c.*236A>G
|
XP_016880302.1:n.*236A>G
|
|
NM_018129.4:c.*236A>G
MANE Select
|
NP_060599.1:n.*236A>G
|
|