ENST00000264381.8:c.1555C>T
MANE Select
|
ENSP00000264381.3:p.Pro519Ser
|
|
ENST00000264381.7:c.1555C>T
|
ENSP00000264381.3:p.Pro519Ser
|
|
ENST00000479451.5:c.145C>T
|
ENSP00000418325.1:p.Pro49Ser
|
|
ENST00000482958.1:c.*61C>T
|
ENSP00000419804.1:n.*61C>T
|
|
ENST00000488954.1:c.145C>T
|
ENSP00000418504.1:p.Pro49Ser
|
|
ENST00000497011.5:c.1555C>T
|
ENSP00000419505.1:p.Pro519Ser
|
|
NM_000055.2:c.1555C>T
|
NP_000046.1:p.Pro519Ser
|
|
XM_005247685.1:c.1678C>T
|
XP_005247742.1:p.Pro560Ser
|
|
NM_000055.3:c.1555C>T
|
NP_000046.1:p.Pro519Ser
|
|
NR_137635.1:n.197C>T
|
|
|
NR_137636.1:n.1722C>T
|
|
|
NM_000055.4:c.1555C>T
MANE Select
|
NP_000046.1:p.Pro519Ser
|
|
NR_137635.2:n.148C>T
|
|
|
NR_137636.2:n.1673C>T
|
|
|