ENST00000379757.9:c.963+770G>A
(TXNDC5)
MANE Select
|
ENSP00000369081.4:n.963+770G>A
|
|
ENST00000379757.8:c.963+770G>A
(TXNDC5)
|
ENSP00000369081.4:n.963+770G>A
|
|
ENST00000439343.2:c.1072+770G>A
(BLOC1S5-TXNDC5)
|
ENSP00000454697.1:n.1072+770G>A
|
|
ENST00000460138.5:n.741+770G>A
(TXNDC5)
|
|
|
ENST00000473453.2:c.639+770G>A
(TXNDC5)
|
ENSP00000420784.1:n.639+770G>A
|
|
ENST00000475802.1:n.257+770G>A
(TXNDC5)
|
|
|
NM_001145549.2:c.639+770G>A
(TXNDC5)
|
NP_001139021.1:n.639+770G>A
|
|
NM_030810.3:c.963+770G>A
(TXNDC5)
|
NP_110437.2:n.963+770G>A
|
|
NR_037616.1:n.1122+770G>A
(BLOC1S5-TXNDC5)
|
|
|
NM_001145549.3:c.639+770G>A
(TXNDC5)
|
NP_001139021.1:n.639+770G>A
|
|
NM_030810.4:c.963+770G>A
(TXNDC5)
|
NP_110437.2:n.963+770G>A
|
|
NM_030810.5:c.963+770G>A
(TXNDC5)
MANE Select
|
NP_110437.2:n.963+770G>A
|
|
NM_001145549.4:c.639+770G>A
(TXNDC5)
|
NP_001139021.1:n.639+770G>A
|
|