ENST00000703783.1:n.1046T>A
|
|
|
ENST00000703785.1:n.1127T>A
|
|
|
ENST00000262464.9:c.4262T>A
MANE Select
|
ENSP00000262464.4:p.Ile1421Asn
|
|
ENST00000262464.8:c.4262T>A
|
ENSP00000262464.4:p.Ile1421Asn
|
|
ENST00000507835.5:c.812T>A
|
ENSP00000426839.1:p.Ile271Asn
|
|
ENST00000508053.5:c.4262T>A
|
ENSP00000424571.1:p.Ile1421Asn
|
|
ENST00000508989.5:c.4163T>A
|
ENSP00000425596.1:p.Ile1388Asn
|
|
ENST00000619499.4:c.4259T>A
|
ENSP00000482132.1:p.Ile1420Asn
|
|
NM_001999.3:c.4262T>A
|
NP_001990.2:p.Ile1421Asn
|
|
XM_017009228.2:c.4109T>A
|
XP_016864717.1:p.Ile1370Asn
|
|
NM_001999.4:c.4262T>A
MANE Select
|
NP_001990.2:p.Ile1421Asn
|
|