ENST00000371270.6:c.408G>T
MANE Select
|
ENSP00000360317.3:p.Met136Ile
|
|
ENST00000371270.5:c.408G>T
|
ENSP00000360317.3:p.Met136Ile
|
|
ENST00000479946.2:n.712G>T
|
|
|
ENST00000490994.6:c.*194G>T
|
ENSP00000433314.1:n.*194G>T
|
|
ENST00000525991.5:c.283G>T
|
ENSP00000433842.1:p.Gly95Trp
|
|
ENST00000526814.5:n.663G>T
|
|
|
ENST00000527420.5:c.408G>T
|
ENSP00000433191.1:p.Met136Ile
|
|
ENST00000527953.5:n.663G>T
|
|
|
ENST00000533320.5:n.642G>T
|
|
|
ENST00000535898.5:c.102G>T
|
ENSP00000445062.1:p.Met34Ile
|
|
ENST00000539050.5:c.198G>T
|
ENSP00000442343.2:p.Met66Ile
|
|
ENST00000623108.3:c.198G>T
|
ENSP00000485110.1:p.Met66Ile
|
|
ENST00000628935.1:c.150G>T
|
ENSP00000487145.1:p.Met50Ile
|
|
NM_000770.3:c.408G>T
MANE Select
|
NP_000761.3:p.Met136Ile
|
|
NM_001198853.1:c.198G>T
|
NP_001185782.1:p.Met66Ile
|
|
NM_001198854.1:c.102G>T
|
NP_001185783.1:p.Met34Ile
|
|
NM_001198855.1:c.198G>T
|
NP_001185784.1:p.Met66Ile
|
|
XR_945610.1:n.504G>T
|
|
|