ENST00000320031.13:c.1675-89A>C
MANE Select
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ENSP00000315190.8:n.1675-89A>C
|
|
ENST00000007722.11:c.1675-89A>C
|
ENSP00000007722.7:n.1675-89A>C
|
|
ENST00000320031.12:c.1675-89A>C
|
ENSP00000315190.8:n.1675-89A>C
|
|
ENST00000505306.5:n.2047-89A>C
|
|
|
ENST00000505612.1:n.277-89A>C
|
|
|
ENST00000506401.6:c.*1068-89A>C
|
ENSP00000422826.2:n.*1068-89A>C
|
|
NM_002204.2:c.1675-89A>C
|
NP_002195.1:n.1675-89A>C
|
|
NM_002204.3:c.1675-89A>C
|
NP_002195.1:n.1675-89A>C
|
|
NM_005501.2:c.1675-89A>C
|
NP_005492.1:n.1675-89A>C
|
|
XM_005257308.1:c.1270-89A>C
|
XP_005257365.1:n.1270-89A>C
|
|
XM_005257308.2:c.1270-89A>C
|
XP_005257365.1:n.1270-89A>C
|
|
XR_001752507.1:n.2050-89A>C
|
|
|
NM_002204.4:c.1675-89A>C
MANE Select
|
NP_002195.1:n.1675-89A>C
|
|