ENST00000710853.1:c.1714G>T
|
ENSP00000518526.1:p.Ala572Ser
|
|
ENST00000361204.9:c.1804G>T
MANE Select
|
ENSP00000354476.4:p.Ala602Ser
|
|
ENST00000361204.8:c.1804G>T
|
ENSP00000354476.4:p.Ala602Ser
|
|
ENST00000424354.5:c.1904G>T
|
ENSP00000395728.1:p.Gly635Val
|
|
ENST00000612482.4:c.1814G>T
|
ENSP00000484441.1:p.Gly605Val
|
|
NM_004599.3:c.1804G>T
|
NP_004590.2:p.Ala602Ser
|
|
NR_103834.1:n.2096G>T
|
|
|
XM_006724310.1:c.1714G>T
|
XP_006724373.1:p.Ala572Ser
|
|
XM_011530347.1:c.1429G>T
|
XP_011528649.1:p.Ala477Ser
|
|
XM_006724310.3:c.1714G>T
|
XP_006724373.1:p.Ala572Ser
|
|
XM_011530347.2:c.1429G>T
|
XP_011528649.1:p.Ala477Ser
|
|
XM_017028921.2:c.1804G>T
|
XP_016884410.1:p.Ala602Ser
|
|
XM_017028922.2:c.1804G>T
|
XP_016884411.1:p.Ala602Ser
|
|
XR_001755276.2:n.1947G>T
|
|
|
XR_001755277.2:n.1947G>T
|
|
|
XR_001755278.2:n.2070G>T
|
|
|
NM_004599.4:c.1804G>T
MANE Select
|
NP_004590.2:p.Ala602Ser
|
|
NR_103834.2:n.2070G>T
|
|
|