ENST00000336411.7:c.1358A>T
|
ENSP00000337915.3:p.Lys453Met
|
|
ENST00000651162.1:n.700A>T
|
|
|
ENST00000651514.1:c.1265A>T
MANE Select
|
ENSP00000498939.1:p.Lys422Met
|
|
ENST00000651783.1:c.806A>T
|
ENSP00000498924.1:p.Lys269Met
|
|
ENST00000652018.1:c.1118A>T
|
ENSP00000498733.1:p.Lys373Met
|
|
ENST00000336411.6:c.1265A>T
|
ENSP00000337915.2:p.Lys422Met
|
|
ENST00000354593.6:c.815A>T
|
ENSP00000346607.2:p.Lys272Met
|
|
NM_001202855.2:c.1262A>T
|
NP_001189784.1:p.Lys421Met
|
|
NM_017460.5:c.1265A>T
|
NP_059488.2:p.Lys422Met
|
|
XM_011515841.1:c.1358A>T
|
XP_011514143.1:p.Lys453Met
|
|
XM_011515842.1:c.1355A>T
|
XP_011514144.1:p.Lys452Met
|
|
NM_017460.6:c.1265A>T
MANE Select
|
NP_059488.2:p.Lys422Met
|
|
NM_001202855.3:c.1262A>T
|
NP_001189784.1:p.Lys421Met
|
|