ENST00000252102.9:c.39G>T
(NDUFA2)
MANE Select
|
ENSP00000252102.5:p.Lys13Asn
|
|
ENST00000252102.8:c.39G>T
(NDUFA2)
|
ENSP00000252102.4:p.Lys13Asn
|
|
ENST00000502960.1:n.227G>T
(NDUFA2)
|
|
|
ENST00000512088.1:c.39G>T
(NDUFA2)
|
ENSP00000427220.1:p.Lys13Asn
|
|
ENST00000513256.5:c.4+236C>A
(IK)
|
ENSP00000425564.1:n.4+236C>A
|
|
NM_001185012.1:c.39G>T
(NDUFA2)
|
NP_001171941.1:p.Lys13Asn
|
|
NM_002488.4:c.39G>T
(NDUFA2)
|
NP_002479.1:p.Lys13Asn
|
|
NR_033697.1:n.241G>T
(NDUFA2)
|
|
|
NM_002488.5:c.39G>T
(NDUFA2)
MANE Select
|
NP_002479.1:p.Lys13Asn
|
|
NM_001185012.2:c.39G>T
(NDUFA2)
|
NP_001171941.1:p.Lys13Asn
|
|
NR_033697.2:n.86G>T
(NDUFA2)
|
|
|