ENST00000368019.5:c.-71G>T
|
ENSP00000356998.1:n.-71G>T
|
|
ENST00000368020.5:c.-71G>T
|
ENSP00000356999.1:n.-71G>T
|
|
ENST00000368021.7:c.-71G>T
MANE Select
|
ENSP00000357000.3:n.-71G>T
|
|
ENST00000473969.6:c.-71G>T
|
ENSP00000435671.1:n.-71G>T
|
|
ENST00000491629.5:n.66G>T
|
|
|
ENST00000496363.5:n.70G>T
|
|
|
ENST00000529476.1:n.97G>T
|
|
|
ENST00000534633.5:c.-263G>T
|
ENSP00000432533.1:n.-263G>T
|
|
NM_001276373.1:c.-71G>T
|
NP_001263302.1:n.-71G>T
|
|
NM_007122.4:c.-71G>T
|
NP_009053.1:n.-71G>T
|
|
NM_207005.2:c.-217G>T
|
NP_996888.1:n.-217G>T
|
|
NM_007122.5:c.-71G>T
MANE Select
|
NP_009053.1:n.-71G>T
|
|
NM_001276373.2:c.-71G>T
|
NP_001263302.1:n.-71G>T
|
|
NM_207005.3:c.-217G>T
|
NP_996888.1:n.-217G>T
|
|