|
ENST00000361492.9:c.2284C>T
MANE Select
|
ENSP00000354586.5:p.Pro762Ser
|
|
|
ENST00000452319.6:c.2335C>T
|
ENSP00000390436.1:p.Pro779Ser
|
|
|
ENST00000314490.15:c.1346C>T
|
ENSP00000312694.12:p.Ala449Val
|
|
|
ENST00000341310.10:c.*1383C>T
|
ENSP00000344473.6:n.*1383C>T
|
|
|
ENST00000361492.8:c.2335C>T
|
ENSP00000354586.4:p.Pro779Ser
|
|
|
ENST00000437950.5:c.*1434C>T
|
ENSP00000415773.1:n.*1434C>T
|
|
|
ENST00000438299.5:c.*1434C>T
|
ENSP00000400593.1:n.*1434C>T
|
|
|
ENST00000445186.5:c.*1434C>T
|
ENSP00000397488.1:n.*1434C>T
|
|
|
ENST00000452319.5:c.2335C>T
|
ENSP00000390436.1:p.Pro779Ser
|
|
|
ENST00000452692.5:c.*1383C>T
|
ENSP00000403715.1:n.*1383C>T
|
|
|
NM_005270.4:c.2335C>T
|
NP_005261.2:p.Pro779Ser
|
|
|
XM_006712422.1:c.2284C>T
|
XP_006712485.1:p.Pro762Ser
|
|
|
XM_011510969.1:c.2317C>T
|
XP_011509271.1:p.Pro773Ser
|
|
|
XM_011510970.1:c.2194C>T
|
XP_011509272.1:p.Pro732Ser
|
|
|
XM_011510971.1:c.2140C>T
|
XP_011509273.1:p.Pro714Ser
|
|
|
XM_011510972.1:c.2140C>T
|
XP_011509274.1:p.Pro714Ser
|
|
|
XM_011510973.1:c.1960C>T
|
XP_011509275.1:p.Pro654Ser
|
|
|
XM_011510974.1:c.1909C>T
|
XP_011509276.1:p.Pro637Ser
|
|
|
XM_006712422.3:c.2284C>T
|
XP_006712485.1:p.Pro762Ser
|
|
|
XM_011510969.2:c.2587C>T
|
XP_011509271.2:p.Pro863Ser
|
|
|
XM_011510970.2:c.2194C>T
|
XP_011509272.1:p.Pro732Ser
|
|
|
XM_011510971.2:c.2140C>T
|
XP_011509273.1:p.Pro714Ser
|
|
|
XM_011510972.2:c.2236C>T
|
XP_011509274.2:p.Pro746Ser
|
|
|
XM_011510973.2:c.1960C>T
|
XP_011509275.1:p.Pro654Ser
|
|
|
XM_011510974.2:c.1909C>T
|
XP_011509276.1:p.Pro637Ser
|
|
|
XM_017003818.1:c.2536C>T
|
XP_016859307.1:p.Pro846Ser
|
|
|
XM_024452794.1:c.2335C>T
|
XP_024308562.1:p.Pro779Ser
|
|
|
XM_024452795.1:c.2335C>T
|
XP_024308563.1:p.Pro779Ser
|
|
|
NM_001371271.1:c.2335C>T
|
NP_001358200.1:p.Pro779Ser
|
|
|
NM_001374353.1:c.2284C>T
MANE Select
|
NP_001361282.1:p.Pro762Ser
|
|
|
NM_001374354.1:c.1909C>T
|
NP_001361283.1:p.Pro637Ser
|
|
|
NM_005270.5:c.2335C>T
|
NP_005261.2:p.Pro779Ser
|
|
