ENST00000297615.10:c.42+17803G>T
|
ENSP00000297615.6:n.42+17803G>T
|
|
ENST00000380850.9:c.42+17803G>T
|
ENSP00000370231.5:n.42+17803G>T
|
|
ENST00000512701.7:c.42+17803G>T
MANE Select
|
ENSP00000422496.2:n.42+17803G>T
|
|
ENST00000297615.9:c.240+17803G>T
|
ENSP00000297615.5:n.240+17803G>T
|
|
ENST00000380850.8:c.240+17803G>T
|
ENSP00000370231.4:n.240+17803G>T
|
|
ENST00000505732.5:n.277+17803G>T
|
|
|
ENST00000506891.1:c.126+17803G>T
|
ENSP00000427314.1:n.126+17803G>T
|
|
ENST00000512701.6:c.240+17803G>T
|
ENSP00000422496.1:n.240+17803G>T
|
|
NM_001168339.1:c.240+17803G>T
|
NP_001161811.1:n.240+17803G>T
|
|
NM_001168340.1:c.240+17803G>T
|
NP_001161812.1:n.240+17803G>T
|
|
NM_001168341.1:c.240+17803G>T
|
NP_001161813.1:n.240+17803G>T
|
|
NM_152574.2:c.240+17803G>T
|
NP_689787.2:n.240+17803G>T
|
|
XM_011517733.1:c.240+17803G>T
|
XP_011516035.1:n.240+17803G>T
|
|
XM_017014310.1:c.-113+10069G>T
|
XP_016869799.1:n.-113+10069G>T
|
|
XM_017014311.1:c.-222+10069G>T
|
XP_016869800.1:n.-222+10069G>T
|
|
XM_024447422.1:c.-52+10069G>T
|
XP_024303190.1:n.-52+10069G>T
|
|
XR_001746190.1:n.277+17803G>T
|
|
|
NM_001168339.2:c.42+17803G>T
|
NP_001161811.2:n.42+17803G>T
|
|
NM_001168340.2:c.42+17803G>T
|
NP_001161812.2:n.42+17803G>T
|
|
NM_001168341.2:c.42+17803G>T
|
NP_001161813.2:n.42+17803G>T
|
|
NM_152574.3:c.42+17803G>T
MANE Select
|
NP_689787.3:n.42+17803G>T
|
|