ENST00000706989.1:c.2181T>A
|
ENSP00000516702.1:p.Pro727=
|
|
ENST00000359125.7:c.2127T>A
MANE Select
|
ENSP00000352035.2:p.Pro709=
|
|
ENST00000637193.1:c.1524T>A
|
ENSP00000490734.1:p.Pro508=
|
|
ENST00000344462.8:c.2034T>A
|
ENSP00000339611.4:p.Pro678=
|
|
ENST00000357249.6:c.1695T>A
|
ENSP00000349789.3:p.Pro565=
|
|
ENST00000359125.6:c.2127T>A
|
ENSP00000352035.2:p.Pro709=
|
|
ENST00000360480.7:c.2043T>A
|
ENSP00000353668.3:p.Pro681=
|
|
ENST00000370224.5:c.2151T>A
|
ENSP00000359244.2:p.Pro717=
|
|
ENST00000625514.2:c.2115T>A
|
ENSP00000486040.1:p.Pro705=
|
|
ENST00000626839.2:c.2073T>A
|
ENSP00000486706.1:p.Pro691=
|
|
ENST00000629241.2:c.2043T>A
|
ENSP00000487142.1:p.Pro681=
|
|
ENST00000629676.2:c.1680-6293T>A
|
ENSP00000486194.1:n.1680-6293T>A
|
|
NM_004518.4:c.2043T>A
|
NP_004509.2:p.Pro681=
|
|
NM_172106.1:c.2073T>A
|
NP_742104.1:p.Pro691=
|
|
NM_172107.2:c.2127T>A
|
NP_742105.1:p.Pro709=
|
|
NM_172108.3:c.2034T>A
|
NP_742106.1:p.Pro678=
|
|
XM_006723787.1:c.2169T>A
|
XP_006723850.1:p.Pro723=
|
|
XM_011528807.1:c.2235T>A
|
XP_011527109.1:p.Pro745=
|
|
XM_011528808.1:c.2232T>A
|
XP_011527110.1:p.Pro744=
|
|
XM_011528809.1:c.2205T>A
|
XP_011527111.1:p.Pro735=
|
|
XM_011528810.1:c.2181T>A
|
XP_011527112.1:p.Pro727=
|
|
XM_011528811.1:c.2151T>A
|
XP_011527113.1:p.Pro717=
|
|
XM_011528812.1:c.2124T>A
|
XP_011527114.1:p.Pro708=
|
|
XM_011528813.1:c.2109T>A
|
XP_011527115.1:p.Pro703=
|
|
XM_011528814.1:c.1716T>A
|
XP_011527116.1:p.Pro572=
|
|
NM_004518.5:c.2043T>A
|
NP_004509.2:p.Pro681=
|
|
NM_172106.2:c.2073T>A
|
NP_742104.1:p.Pro691=
|
|
NM_172107.3:c.2127T>A
|
NP_742105.1:p.Pro709=
|
|
NM_172108.4:c.2034T>A
|
NP_742106.1:p.Pro678=
|
|
XM_011528810.2:c.2181T>A
|
XP_011527112.1:p.Pro727=
|
|
XM_011528811.2:c.2151T>A
|
XP_011527113.1:p.Pro717=
|
|
XM_017027841.2:c.2178T>A
|
XP_016883330.1:p.Pro726=
|
|
XM_017027842.2:c.2115T>A
|
XP_016883331.1:p.Pro705=
|
|
XM_017027843.1:c.2112T>A
|
XP_016883332.1:p.Pro704=
|
|
XM_017027844.2:c.2070T>A
|
XP_016883333.1:p.Pro690=
|
|
XM_017027845.1:c.1143T>A
|
XP_016883334.1:p.Pro381=
|
|
NM_004518.6:c.2043T>A
|
NP_004509.2:p.Pro681=
|
|
NM_172106.3:c.2073T>A
|
NP_742104.1:p.Pro691=
|
|
NM_172107.4:c.2127T>A
MANE Select
|
NP_742105.1:p.Pro709=
|
|
NM_172108.5:c.2034T>A
|
NP_742106.1:p.Pro678=
|
|
NM_001382235.1:c.2181T>A
|
NP_001369164.1:p.Pro727=
|
|