ENST00000343164.9:c.471G>A
MANE Select
|
ENSP00000339260.4:p.Trp157Ter
|
|
ENST00000343164.8:c.471G>A
|
ENSP00000339260.4:p.Trp157Ter
|
|
ENST00000445055.6:c.203-4611G>A
|
ENSP00000407104.2:n.203-4611G>A
|
|
ENST00000536842.5:n.524G>A
|
|
|
ENST00000539260.1:c.*110G>A
|
ENSP00000437386.1:n.*110G>A
|
|
ENST00000542272.5:c.114G>A
|
ENSP00000443466.1:p.Trp38Ter
|
|
ENST00000546319.5:c.203-4611G>A
|
ENSP00000444606.1:n.203-4611G>A
|
|
NM_001190997.2:c.203-4611G>A
|
NP_001177926.1:n.203-4611G>A
|
|
NM_016615.4:c.471G>A
|
NP_057699.2:p.Trp157Ter
|
|
XM_005253749.2:c.537G>A
|
XP_005253806.1:p.Trp179Ter
|
|
XM_011521012.1:c.114G>A
|
XP_011519314.1:p.Trp38Ter
|
|
XM_011521013.1:c.-189G>A
|
XP_011519315.1:n.-189G>A
|
|
XM_011521014.1:c.-189G>A
|
XP_011519316.1:n.-189G>A
|
|
XM_011521012.2:c.114G>A
|
XP_011519314.1:p.Trp38Ter
|
|
XM_017019844.1:c.471G>A
|
XP_016875333.1:p.Trp157Ter
|
|
XM_017019846.1:c.471G>A
|
XP_016875335.1:p.Trp157Ter
|
|
XM_017019847.1:c.471G>A
|
XP_016875336.1:p.Trp157Ter
|
|
XR_001748849.1:n.524G>A
|
|
|
XR_002957372.1:n.524G>A
|
|
|
NM_016615.5:c.471G>A
MANE Select
|
NP_057699.2:p.Trp157Ter
|
|
NM_001190997.3:c.203-4611G>A
|
NP_001177926.1:n.203-4611G>A
|
|