ENST00000371270.6:c.1414G>T
MANE Select
|
ENSP00000360317.3:p.Val472Phe
|
|
ENST00000371270.5:c.1414G>T
|
ENSP00000360317.3:p.Val472Phe
|
|
ENST00000490994.6:c.*1200G>T
|
ENSP00000433314.1:n.*1200G>T
|
|
ENST00000525991.5:c.*989G>T
|
ENSP00000433842.1:n.*989G>T
|
|
ENST00000526814.5:n.1669G>T
|
|
|
ENST00000527420.5:c.*271G>T
|
ENSP00000433191.1:n.*271G>T
|
|
ENST00000527953.5:n.1708G>T
|
|
|
ENST00000531714.1:n.602G>T
|
|
|
ENST00000533320.5:n.1648G>T
|
|
|
ENST00000535898.5:c.1108G>T
|
ENSP00000445062.1:p.Val370Phe
|
|
ENST00000539050.5:c.1204G>T
|
ENSP00000442343.2:p.Val402Phe
|
|
ENST00000623108.3:c.1204G>T
|
ENSP00000485110.1:p.Val402Phe
|
|
NM_000770.3:c.1414G>T
MANE Select
|
NP_000761.3:p.Val472Phe
|
|
NM_001198853.1:c.1204G>T
|
NP_001185782.1:p.Val402Phe
|
|
NM_001198854.1:c.1108G>T
|
NP_001185783.1:p.Val370Phe
|
|
NM_001198855.1:c.1204G>T
|
NP_001185784.1:p.Val402Phe
|
|
XR_945610.1:n.1549G>T
|
|
|